Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522194T>C , CM000671.2:g.131522194T>C	GRCh38
NC_000009.11:g.134397581T>C , CM000671.1:g.134397581T>C	GRCh37
NC_000009.10:g.133387402T>C	NCBI36
NG_008896.1:g.24293T>C
NG_008896.2:g.24293T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.1811T>C	ENSP00000343034.7:p.Val604Ala
ENST00000404875.7:n.2513T>C
ENST00000423007.6:c.2030T>C	ENSP00000404119.2:p.Val677Ala
ENST00000677295.2:c.*2317T>C	ENSP00000504346.2:n.*2317T>C
ENST00000678264.2:c.*2156T>C	ENSP00000503157.2:n.*2156T>C
ENST00000682070.1:n.2291-8T>C
ENST00000682813.1:n.2377T>C
ENST00000683392.1:n.4573-8T>C
ENST00000683712.1:n.2378T>C
ENST00000683900.1:n.3873T>C
ENST00000684062.1:n.2639T>C
ENST00000684579.1:n.3819T>C
ENST00000684679.1:n.1200T>C
ENST00000341012.12:c.1811T>C	ENSP00000343034.7:p.Val604Ala
ENST00000372220.5:c.842T>C	ENSP00000361294.5:p.Val281Ala
ENST00000372228.9:c.2039T>C	ENSP00000361302.3:p.Val680Ala
ENST00000402686.8:c.1973T>C MANE Select	ENSP00000385797.4:p.Val658Ala
ENST00000676640.1:c.1973T>C	ENSP00000503281.1:p.Val658Ala
ENST00000676803.1:c.1034T>C	ENSP00000503093.1:p.Val345Ala
ENST00000676835.1:c.*1188T>C	ENSP00000502911.1:n.*1188T>C
ENST00000677029.1:c.1517T>C	ENSP00000502936.1:p.Val506Ala
ENST00000677099.1:c.*1683T>C	ENSP00000504553.1:n.*1683T>C
ENST00000677216.1:c.1622T>C	ENSP00000503772.1:p.Val541Ala
ENST00000677221.1:n.998T>C
ENST00000677295.1:c.*1203-8T>C	ENSP00000504346.1:n.*1203-8T>C
ENST00000677444.1:c.1918T>C
ENST00000677586.1:n.1340T>C
ENST00000677626.1:c.1622T>C	ENSP00000503552.1:p.Val541Ala
ENST00000677853.1:c.*981T>C	ENSP00000503488.1:n.*981T>C
ENST00000678202.1:n.1132T>C
ENST00000678264.1:c.*1350T>C	ENSP00000503157.1:n.*1350T>C
ENST00000678303.1:c.1883T>C	ENSP00000503696.1:p.Val628Ala
ENST00000678366.1:c.*2222T>C	ENSP00000504353.1:n.*2222T>C
ENST00000678546.1:c.*1918T>C	ENSP00000503062.1:n.*1918T>C
ENST00000678548.1:c.*2112T>C	ENSP00000503934.1:n.*2112T>C
ENST00000678626.1:n.1809T>C
ENST00000678739.1:c.*2147-8T>C	ENSP00000503806.1:n.*2147-8T>C
ENST00000678833.1:c.*1725T>C	ENSP00000503893.1:n.*1725T>C
ENST00000679023.1:c.1811T>C	ENSP00000503718.1:p.Val604Ala
ENST00000679076.1:c.1592T>C
ENST00000679111.1:c.*729T>C	ENSP00000504257.1:n.*729T>C
ENST00000679189.1:c.1622T>C	ENSP00000503356.1:p.Val541Ala
ENST00000341012.11:c.1811T>C	ENSP00000343034.7:p.Val604Ala
ENST00000372220.4:c.836T>C	ENSP00000361294.4:p.Val279Ala
ENST00000372228.7:c.2039T>C	ENSP00000361302.3:p.Val680Ala
ENST00000402686.7:c.1973T>C	ENSP00000385797.3:p.Val658Ala
ENST00000404875.6:c.1622T>C	ENSP00000384531.2:p.Val541Ala
ENST00000423007.5:c.1973T>C	ENSP00000404119.1:p.Val658Ala
ENST00000485278.5:n.2523T>C
ENST00000494883.1:n.516T>C
NM_001077365.1:c.1973T>C	NP_001070833.1:p.Val658Ala
NM_001077366.1:c.1811T>C	NP_001070834.1:p.Val604Ala
NM_001136113.1:c.1973T>C	NP_001129585.1:p.Val658Ala
NM_001136114.1:c.1622T>C	NP_001129586.1:p.Val541Ala
NM_007171.3:c.2039T>C	NP_009102.3:p.Val680Ala
XM_005272156.1:c.2039T>C	XP_005272213.1:p.Val680Ala
XM_005272158.1:c.1877T>C	XP_005272215.1:p.Val626Ala
XM_005272159.1:c.1688T>C	XP_005272216.1:p.Val563Ala
XM_005272162.1:c.842T>C	XP_005272219.1:p.Val281Ala
XM_006716932.1:c.1688T>C	XP_006716995.1:p.Val563Ala
XM_011518140.1:c.1892T>C	XP_011516442.1:p.Val631Ala
XM_011518141.1:c.1826T>C	XP_011516443.1:p.Val609Ala
XM_011518142.1:c.1730T>C	XP_011516444.1:p.Val577Ala
XM_011518143.1:c.1724T>C	XP_011516445.1:p.Val575Ala
XM_011518145.1:c.1583T>C	XP_011516447.1:p.Val528Ala
XM_011518147.1:c.911T>C	XP_011516449.1:p.Val304Ala
XR_929703.1:n.2215T>C
NM_001353193.1:c.2039T>C	NP_001340122.1:p.Val680Ala
NM_001353194.1:c.1811T>C	NP_001340123.1:p.Val604Ala
NM_001353195.1:c.1622T>C	NP_001340124.1:p.Val541Ala
NM_001353196.1:c.1883T>C	NP_001340125.1:p.Val628Ala
NM_001353197.1:c.1877T>C	NP_001340126.1:p.Val626Ala
NM_001353198.1:c.1877T>C	NP_001340127.1:p.Val626Ala
NM_001353199.1:c.1688T>C	NP_001340128.1:p.Val563Ala
NM_001353200.1:c.1517T>C	NP_001340129.1:p.Val506Ala
NR_148391.1:n.2023T>C
NR_148392.1:n.2241T>C
NR_148393.1:n.2162T>C
NR_148394.1:n.1916T>C
NR_148395.1:n.2314T>C
NR_148396.1:n.1948T>C
NR_148397.1:n.2073T>C
NR_148398.1:n.2028T>C
NR_148399.1:n.2554T>C
NR_148400.1:n.2153T>C
XM_005272162.3:c.842T>C	XP_005272219.1:p.Val281Ala
XM_006716932.2:c.1688T>C	XP_006716995.1:p.Val563Ala
XM_011518140.2:c.1892T>C	XP_011516442.1:p.Val631Ala
XM_011518141.2:c.1826T>C	XP_011516443.1:p.Val609Ala
XM_011518142.2:c.1730T>C	XP_011516444.1:p.Val577Ala
XM_011518143.2:c.1724T>C	XP_011516445.1:p.Val575Ala
XM_011518145.2:c.1583T>C	XP_011516447.1:p.Val528Ala
XM_017014205.2:c.842T>C	XP_016869694.1:p.Val281Ala
XM_024447380.1:c.842T>C	XP_024303148.1:p.Val281Ala
XM_024447381.1:c.1148T>C	XP_024303149.1:p.Val383Ala
XM_024447382.1:c.842T>C	XP_024303150.1:p.Val281Ala
XR_001746160.2:n.2143T>C
XR_001746162.2:n.2348T>C
XR_001746164.1:n.2065T>C
XR_001746166.2:n.2360T>C
NM_001077365.2:c.1973T>C MANE Select	NP_001070833.1:p.Val658Ala
NM_001077366.2:c.1811T>C	NP_001070834.1:p.Val604Ala
NM_001136113.2:c.1973T>C	NP_001129585.1:p.Val658Ala
NM_001136114.2:c.1622T>C	NP_001129586.1:p.Val541Ala
NM_001353193.2:c.2039T>C	NP_001340122.2:p.Val680Ala
NM_001353194.2:c.1811T>C	NP_001340123.1:p.Val604Ala
NM_001353195.2:c.1622T>C	NP_001340124.1:p.Val541Ala
NM_001353196.2:c.1883T>C	NP_001340125.1:p.Val628Ala
NM_001353197.2:c.1877T>C	NP_001340126.2:p.Val626Ala
NM_001353198.2:c.1877T>C	NP_001340127.2:p.Val626Ala
NM_001353199.2:c.1688T>C	NP_001340128.2:p.Val563Ala
NM_001353200.2:c.1517T>C	NP_001340129.1:p.Val506Ala
NM_001374689.1:c.1961T>C	NP_001361618.1:p.Val654Ala
NM_001374690.1:c.1754T>C	NP_001361619.1:p.Val585Ala
NM_001374691.1:c.1622T>C	NP_001361620.1:p.Val541Ala
NM_001374692.1:c.1622T>C	NP_001361621.1:p.Val541Ala
NM_001374693.1:c.1622T>C	NP_001361622.1:p.Val541Ala
NM_001374695.1:c.1583T>C	NP_001361624.1:p.Val528Ala
NM_007171.4:c.2039T>C	NP_009102.4:p.Val680Ala
NR_148391.2:n.2007T>C
NR_148392.2:n.2225T>C
NR_148393.2:n.2146T>C
NR_148394.2:n.1900T>C
NR_148395.2:n.2298T>C
NR_148396.2:n.1932T>C
NR_148397.2:n.2057T>C
NR_148398.2:n.2012T>C
NR_148399.2:n.2538T>C
NR_148400.2:n.2137T>C

Linked Data

Genomic Alleles

Transcript Alleles