Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131523066G>C , CM000671.2:g.131523066G>C	GRCh38
NC_000009.11:g.134398453G>C , CM000671.1:g.134398453G>C	GRCh37
NC_000009.10:g.133388274G>C	NCBI36
NG_008896.1:g.25165G>C
NG_008896.2:g.25165G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000341012.13:c.1976G>C	ENSP00000343034.7:p.Arg659Pro
ENST00000404875.7:n.2678G>C
ENST00000423007.6:c.2195G>C	ENSP00000404119.2:p.Arg732Pro
ENST00000677295.2:c.*2482G>C	ENSP00000504346.2:n.*2482G>C
ENST00000678264.2:c.*2321G>C	ENSP00000503157.2:n.*2321G>C
ENST00000682070.1:n.2448G>C
ENST00000682639.1:c.135G>C
ENST00000682813.1:n.2535G>C
ENST00000683231.1:c.135G>C
ENST00000683392.1:n.4730G>C
ENST00000683712.1:n.2543G>C
ENST00000683900.1:n.4038G>C
ENST00000684062.1:n.2804G>C
ENST00000684399.1:c.135G>C
ENST00000684579.1:n.3984G>C
ENST00000341012.12:c.1976G>C	ENSP00000343034.7:p.Arg659Pro
ENST00000372220.5:c.1007G>C	ENSP00000361294.5:p.Arg336Pro
ENST00000372228.9:c.2204G>C	ENSP00000361302.3:p.Arg735Pro
ENST00000402686.8:c.2138G>C MANE Select	ENSP00000385797.4:p.Arg713Pro
ENST00000676640.1:c.2138G>C	ENSP00000503281.1:p.Arg713Pro
ENST00000676803.1:c.1199G>C	ENSP00000503093.1:p.Arg400Pro
ENST00000676835.1:c.*1353G>C	ENSP00000502911.1:n.*1353G>C
ENST00000677029.1:c.1682G>C	ENSP00000502936.1:p.Arg561Pro
ENST00000677099.1:c.*1848G>C	ENSP00000504553.1:n.*1848G>C
ENST00000677216.1:c.1787G>C	ENSP00000503772.1:p.Arg596Pro
ENST00000677295.1:c.*1360G>C	ENSP00000504346.1:n.*1360G>C
ENST00000677444.1:c.2083G>C
ENST00000677586.1:n.1505G>C
ENST00000677626.1:c.1787G>C	ENSP00000503552.1:p.Arg596Pro
ENST00000677853.1:c.*1146G>C	ENSP00000503488.1:n.*1146G>C
ENST00000678264.1:c.*1515G>C	ENSP00000503157.1:n.*1515G>C
ENST00000678303.1:c.2048G>C	ENSP00000503696.1:p.Arg683Pro
ENST00000678366.1:c.*2387G>C	ENSP00000504353.1:n.*2387G>C
ENST00000678546.1:c.*2083G>C	ENSP00000503062.1:n.*2083G>C
ENST00000678548.1:c.*2277G>C	ENSP00000503934.1:n.*2277G>C
ENST00000678626.1:n.1974G>C
ENST00000678739.1:c.*2304G>C	ENSP00000503806.1:n.*2304G>C
ENST00000678833.1:c.*1890G>C	ENSP00000503893.1:n.*1890G>C
ENST00000679023.1:c.1976G>C	ENSP00000503718.1:p.Arg659Pro
ENST00000679076.1:c.1757G>C
ENST00000679111.1:c.*894G>C	ENSP00000504257.1:n.*894G>C
ENST00000679189.1:c.1787G>C	ENSP00000503356.1:p.Arg596Pro
ENST00000341012.11:c.1976G>C	ENSP00000343034.7:p.Arg659Pro
ENST00000372220.4:c.1001G>C	ENSP00000361294.4:p.Arg334Pro
ENST00000372228.7:c.2204G>C	ENSP00000361302.3:p.Arg735Pro
ENST00000402686.7:c.2138G>C	ENSP00000385797.3:p.Arg713Pro
ENST00000404875.6:c.1787G>C	ENSP00000384531.2:p.Arg596Pro
ENST00000423007.5:c.2138G>C	ENSP00000404119.1:p.Arg713Pro
ENST00000485278.5:n.2688G>C
NM_001077365.1:c.2138G>C	NP_001070833.1:p.Arg713Pro
NM_001077366.1:c.1976G>C	NP_001070834.1:p.Arg659Pro
NM_001136113.1:c.2138G>C	NP_001129585.1:p.Arg713Pro
NM_001136114.1:c.1787G>C	NP_001129586.1:p.Arg596Pro
NM_007171.3:c.2204G>C	NP_009102.3:p.Arg735Pro
XM_005272156.1:c.2204G>C	XP_005272213.1:p.Arg735Pro
XM_005272158.1:c.2042G>C	XP_005272215.1:p.Arg681Pro
XM_005272159.1:c.1853G>C	XP_005272216.1:p.Arg618Pro
XM_005272162.1:c.1007G>C	XP_005272219.1:p.Arg336Pro
XM_006716932.1:c.1853G>C	XP_006716995.1:p.Arg618Pro
XM_011518140.1:c.2057G>C	XP_011516442.1:p.Arg686Pro
XM_011518141.1:c.1991G>C	XP_011516443.1:p.Arg664Pro
XM_011518142.1:c.1895G>C	XP_011516444.1:p.Arg632Pro
XM_011518143.1:c.1889G>C	XP_011516445.1:p.Arg630Pro
XM_011518145.1:c.1748G>C	XP_011516447.1:p.Arg583Pro
XM_011518147.1:c.1076G>C	XP_011516449.1:p.Arg359Pro
XR_929703.1:n.2380G>C
NM_001353193.1:c.2204G>C	NP_001340122.1:p.Arg735Pro
NM_001353194.1:c.1976G>C	NP_001340123.1:p.Arg659Pro
NM_001353195.1:c.1787G>C	NP_001340124.1:p.Arg596Pro
NM_001353196.1:c.2048G>C	NP_001340125.1:p.Arg683Pro
NM_001353197.1:c.2042G>C	NP_001340126.1:p.Arg681Pro
NM_001353198.1:c.2042G>C	NP_001340127.1:p.Arg681Pro
NM_001353199.1:c.1853G>C	NP_001340128.1:p.Arg618Pro
NM_001353200.1:c.1682G>C	NP_001340129.1:p.Arg561Pro
NR_148391.1:n.2188G>C
NR_148392.1:n.2406G>C
NR_148393.1:n.2327G>C
NR_148394.1:n.2081G>C
NR_148395.1:n.2479G>C
NR_148396.1:n.2113G>C
NR_148397.1:n.2238G>C
NR_148398.1:n.2193G>C
NR_148399.1:n.2719G>C
NR_148400.1:n.2318G>C
XM_005272162.3:c.1007G>C	XP_005272219.1:p.Arg336Pro
XM_006716932.2:c.1853G>C	XP_006716995.1:p.Arg618Pro
XM_011518140.2:c.2057G>C	XP_011516442.1:p.Arg686Pro
XM_011518141.2:c.1991G>C	XP_011516443.1:p.Arg664Pro
XM_011518142.2:c.1895G>C	XP_011516444.1:p.Arg632Pro
XM_011518143.2:c.1889G>C	XP_011516445.1:p.Arg630Pro
XM_011518145.2:c.1748G>C	XP_011516447.1:p.Arg583Pro
XM_017014205.2:c.1007G>C	XP_016869694.1:p.Arg336Pro
XM_024447380.1:c.1007G>C	XP_024303148.1:p.Arg336Pro
XM_024447381.1:c.1313G>C	XP_024303149.1:p.Arg438Pro
XM_024447382.1:c.1007G>C	XP_024303150.1:p.Arg336Pro
XR_001746160.2:n.2308G>C
XR_001746162.2:n.2513G>C
XR_001746164.1:n.2230G>C
XR_001746166.2:n.2525G>C
NM_001077365.2:c.2138G>C MANE Select	NP_001070833.1:p.Arg713Pro
NM_001077366.2:c.1976G>C	NP_001070834.1:p.Arg659Pro
NM_001136113.2:c.2138G>C	NP_001129585.1:p.Arg713Pro
NM_001136114.2:c.1787G>C	NP_001129586.1:p.Arg596Pro
NM_001353193.2:c.2204G>C	NP_001340122.2:p.Arg735Pro
NM_001353194.2:c.1976G>C	NP_001340123.1:p.Arg659Pro
NM_001353195.2:c.1787G>C	NP_001340124.1:p.Arg596Pro
NM_001353196.2:c.2048G>C	NP_001340125.1:p.Arg683Pro
NM_001353197.2:c.2042G>C	NP_001340126.2:p.Arg681Pro
NM_001353198.2:c.2042G>C	NP_001340127.2:p.Arg681Pro
NM_001353199.2:c.1853G>C	NP_001340128.2:p.Arg618Pro
NM_001353200.2:c.1682G>C	NP_001340129.1:p.Arg561Pro
NM_001374689.1:c.2126G>C	NP_001361618.1:p.Arg709Pro
NM_001374690.1:c.1919G>C	NP_001361619.1:p.Arg640Pro
NM_001374691.1:c.1787G>C	NP_001361620.1:p.Arg596Pro
NM_001374692.1:c.1787G>C	NP_001361621.1:p.Arg596Pro
NM_001374693.1:c.1787G>C	NP_001361622.1:p.Arg596Pro
NM_001374695.1:c.1748G>C	NP_001361624.1:p.Arg583Pro
NM_007171.4:c.2204G>C	NP_009102.4:p.Arg735Pro
NR_148391.2:n.2172G>C
NR_148392.2:n.2390G>C
NR_148393.2:n.2311G>C
NR_148394.2:n.2065G>C
NR_148395.2:n.2463G>C
NR_148396.2:n.2097G>C
NR_148397.2:n.2222G>C
NR_148398.2:n.2177G>C
NR_148399.2:n.2703G>C
NR_148400.2:n.2302G>C

Linked Data

Genomic Alleles

Transcript Alleles