Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522949G>C , CM000671.2:g.131522949G>C	GRCh38
NC_000009.11:g.134398336G>C , CM000671.1:g.134398336G>C	GRCh37
NC_000009.10:g.133388157G>C	NCBI36
NG_008896.1:g.25048G>C
NG_008896.2:g.25048G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.1859G>C	ENSP00000343034.7:p.Ser620Thr
ENST00000404875.7:n.2561G>C
ENST00000423007.6:c.2078G>C	ENSP00000404119.2:p.Ser693Thr
ENST00000677295.2:c.*2365G>C	ENSP00000504346.2:n.*2365G>C
ENST00000678264.2:c.*2204G>C	ENSP00000503157.2:n.*2204G>C
ENST00000682070.1:n.2331G>C
ENST00000682639.1:c.18G>C
ENST00000682813.1:n.2418G>C
ENST00000683231.1:c.18G>C
ENST00000683392.1:n.4613G>C
ENST00000683712.1:n.2426G>C
ENST00000683900.1:n.3921G>C
ENST00000684062.1:n.2687G>C
ENST00000684399.1:c.18G>C
ENST00000684579.1:n.3867G>C
ENST00000341012.12:c.1859G>C	ENSP00000343034.7:p.Ser620Thr
ENST00000372220.5:c.890G>C	ENSP00000361294.5:p.Ser297Thr
ENST00000372228.9:c.2087G>C	ENSP00000361302.3:p.Ser696Thr
ENST00000402686.8:c.2021G>C MANE Select	ENSP00000385797.4:p.Ser674Thr
ENST00000676640.1:c.2021G>C	ENSP00000503281.1:p.Ser674Thr
ENST00000676803.1:c.1082G>C	ENSP00000503093.1:p.Ser361Thr
ENST00000676835.1:c.*1236G>C	ENSP00000502911.1:n.*1236G>C
ENST00000677029.1:c.1565G>C	ENSP00000502936.1:p.Ser522Thr
ENST00000677099.1:c.*1731G>C	ENSP00000504553.1:n.*1731G>C
ENST00000677216.1:c.1670G>C	ENSP00000503772.1:p.Ser557Thr
ENST00000677221.1:n.1046G>C
ENST00000677295.1:c.*1243G>C	ENSP00000504346.1:n.*1243G>C
ENST00000677444.1:c.1966G>C
ENST00000677586.1:n.1388G>C
ENST00000677626.1:c.1670G>C	ENSP00000503552.1:p.Ser557Thr
ENST00000677853.1:c.*1029G>C	ENSP00000503488.1:n.*1029G>C
ENST00000678264.1:c.*1398G>C	ENSP00000503157.1:n.*1398G>C
ENST00000678303.1:c.1931G>C	ENSP00000503696.1:p.Ser644Thr
ENST00000678366.1:c.*2270G>C	ENSP00000504353.1:n.*2270G>C
ENST00000678546.1:c.*1966G>C	ENSP00000503062.1:n.*1966G>C
ENST00000678548.1:c.*2160G>C	ENSP00000503934.1:n.*2160G>C
ENST00000678626.1:n.1857G>C
ENST00000678739.1:c.*2187G>C	ENSP00000503806.1:n.*2187G>C
ENST00000678833.1:c.*1773G>C	ENSP00000503893.1:n.*1773G>C
ENST00000679023.1:c.1859G>C	ENSP00000503718.1:p.Ser620Thr
ENST00000679076.1:c.1640G>C
ENST00000679111.1:c.*777G>C	ENSP00000504257.1:n.*777G>C
ENST00000679189.1:c.1670G>C	ENSP00000503356.1:p.Ser557Thr
ENST00000341012.11:c.1859G>C	ENSP00000343034.7:p.Ser620Thr
ENST00000372220.4:c.884G>C	ENSP00000361294.4:p.Ser295Thr
ENST00000372228.7:c.2087G>C	ENSP00000361302.3:p.Ser696Thr
ENST00000402686.7:c.2021G>C	ENSP00000385797.3:p.Ser674Thr
ENST00000404875.6:c.1670G>C	ENSP00000384531.2:p.Ser557Thr
ENST00000423007.5:c.2021G>C	ENSP00000404119.1:p.Ser674Thr
ENST00000485278.5:n.2571G>C
NM_001077365.1:c.2021G>C	NP_001070833.1:p.Ser674Thr
NM_001077366.1:c.1859G>C	NP_001070834.1:p.Ser620Thr
NM_001136113.1:c.2021G>C	NP_001129585.1:p.Ser674Thr
NM_001136114.1:c.1670G>C	NP_001129586.1:p.Ser557Thr
NM_007171.3:c.2087G>C	NP_009102.3:p.Ser696Thr
XM_005272156.1:c.2087G>C	XP_005272213.1:p.Ser696Thr
XM_005272158.1:c.1925G>C	XP_005272215.1:p.Ser642Thr
XM_005272159.1:c.1736G>C	XP_005272216.1:p.Ser579Thr
XM_005272162.1:c.890G>C	XP_005272219.1:p.Ser297Thr
XM_006716932.1:c.1736G>C	XP_006716995.1:p.Ser579Thr
XM_011518140.1:c.1940G>C	XP_011516442.1:p.Ser647Thr
XM_011518141.1:c.1874G>C	XP_011516443.1:p.Ser625Thr
XM_011518142.1:c.1778G>C	XP_011516444.1:p.Ser593Thr
XM_011518143.1:c.1772G>C	XP_011516445.1:p.Ser591Thr
XM_011518145.1:c.1631G>C	XP_011516447.1:p.Ser544Thr
XM_011518147.1:c.959G>C	XP_011516449.1:p.Ser320Thr
XR_929703.1:n.2263G>C
NM_001353193.1:c.2087G>C	NP_001340122.1:p.Ser696Thr
NM_001353194.1:c.1859G>C	NP_001340123.1:p.Ser620Thr
NM_001353195.1:c.1670G>C	NP_001340124.1:p.Ser557Thr
NM_001353196.1:c.1931G>C	NP_001340125.1:p.Ser644Thr
NM_001353197.1:c.1925G>C	NP_001340126.1:p.Ser642Thr
NM_001353198.1:c.1925G>C	NP_001340127.1:p.Ser642Thr
NM_001353199.1:c.1736G>C	NP_001340128.1:p.Ser579Thr
NM_001353200.1:c.1565G>C	NP_001340129.1:p.Ser522Thr
NR_148391.1:n.2071G>C
NR_148392.1:n.2289G>C
NR_148393.1:n.2210G>C
NR_148394.1:n.1964G>C
NR_148395.1:n.2362G>C
NR_148396.1:n.1996G>C
NR_148397.1:n.2121G>C
NR_148398.1:n.2076G>C
NR_148399.1:n.2602G>C
NR_148400.1:n.2201G>C
XM_005272162.3:c.890G>C	XP_005272219.1:p.Ser297Thr
XM_006716932.2:c.1736G>C	XP_006716995.1:p.Ser579Thr
XM_011518140.2:c.1940G>C	XP_011516442.1:p.Ser647Thr
XM_011518141.2:c.1874G>C	XP_011516443.1:p.Ser625Thr
XM_011518142.2:c.1778G>C	XP_011516444.1:p.Ser593Thr
XM_011518143.2:c.1772G>C	XP_011516445.1:p.Ser591Thr
XM_011518145.2:c.1631G>C	XP_011516447.1:p.Ser544Thr
XM_017014205.2:c.890G>C	XP_016869694.1:p.Ser297Thr
XM_024447380.1:c.890G>C	XP_024303148.1:p.Ser297Thr
XM_024447381.1:c.1196G>C	XP_024303149.1:p.Ser399Thr
XM_024447382.1:c.890G>C	XP_024303150.1:p.Ser297Thr
XR_001746160.2:n.2191G>C
XR_001746162.2:n.2396G>C
XR_001746164.1:n.2113G>C
XR_001746166.2:n.2408G>C
NM_001077365.2:c.2021G>C MANE Select	NP_001070833.1:p.Ser674Thr
NM_001077366.2:c.1859G>C	NP_001070834.1:p.Ser620Thr
NM_001136113.2:c.2021G>C	NP_001129585.1:p.Ser674Thr
NM_001136114.2:c.1670G>C	NP_001129586.1:p.Ser557Thr
NM_001353193.2:c.2087G>C	NP_001340122.2:p.Ser696Thr
NM_001353194.2:c.1859G>C	NP_001340123.1:p.Ser620Thr
NM_001353195.2:c.1670G>C	NP_001340124.1:p.Ser557Thr
NM_001353196.2:c.1931G>C	NP_001340125.1:p.Ser644Thr
NM_001353197.2:c.1925G>C	NP_001340126.2:p.Ser642Thr
NM_001353198.2:c.1925G>C	NP_001340127.2:p.Ser642Thr
NM_001353199.2:c.1736G>C	NP_001340128.2:p.Ser579Thr
NM_001353200.2:c.1565G>C	NP_001340129.1:p.Ser522Thr
NM_001374689.1:c.2009G>C	NP_001361618.1:p.Ser670Thr
NM_001374690.1:c.1802G>C	NP_001361619.1:p.Ser601Thr
NM_001374691.1:c.1670G>C	NP_001361620.1:p.Ser557Thr
NM_001374692.1:c.1670G>C	NP_001361621.1:p.Ser557Thr
NM_001374693.1:c.1670G>C	NP_001361622.1:p.Ser557Thr
NM_001374695.1:c.1631G>C	NP_001361624.1:p.Ser544Thr
NM_007171.4:c.2087G>C	NP_009102.4:p.Ser696Thr
NR_148391.2:n.2055G>C
NR_148392.2:n.2273G>C
NR_148393.2:n.2194G>C
NR_148394.2:n.1948G>C
NR_148395.2:n.2346G>C
NR_148396.2:n.1980G>C
NR_148397.2:n.2105G>C
NR_148398.2:n.2060G>C
NR_148399.2:n.2586G>C
NR_148400.2:n.2185G>C

Linked Data

Genomic Alleles

Transcript Alleles