Canonical Allele Identifier: CA6988674

Gene: ATP7B

Linked Data

• dbSNP Id: rs372318135
• ExAC: 13:52515294 G / A
• gnomAD v2: 13-52515294-G-A
• gnomAD v3: 13-51941158-G-A
• gnomAD v4: 13-51941158-G-A
• MyVariant Identifiers: chr13:g.52515294G>A (hg19) ; chr13:g.51941158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941158G>A , CM000675.2:g.51941158G>A	GRCh38
NC_000013.10:g.52515294G>A , CM000675.1:g.52515294G>A	GRCh37
NC_000013.9:g.51413295G>A	NCBI36
NG_008806.1:g.75337C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1129C>T	ENSP00000489512.2:n.*1129C>T
ENST00000673864.2:c.*2223C>T	ENSP00000501045.2:n.*2223C>T
ENST00000674147.2:c.2858C>T	ENSP00000500964.2:p.Thr953Ile
ENST00000242839.10:c.3479C>T MANE Select	ENSP00000242839.5:p.Thr1160Ile
ENST00000344297.9:c.2858C>T	ENSP00000342559.5:p.Thr953Ile
ENST00000400366.6:c.3146C>T	ENSP00000383217.3:p.Thr1049Ile
ENST00000448424.7:c.3227C>T	ENSP00000416738.3:p.Thr1076Ile
ENST00000673772.1:c.3245C>T	ENSP00000501168.1:p.Thr1082Ile
ENST00000673867.1:n.3618C>T
ENST00000674126.1:n.3842C>T
ENST00000674147.1:c.2414C>T	ENSP00000500964.1:p.Thr805Ile
ENST00000242839.8:c.3479C>T	ENSP00000242839.4:p.Thr1160Ile
ENST00000344297.8:c.2858C>T	ENSP00000342559.5:p.Thr953Ile
ENST00000400366.5:c.3146C>T	ENSP00000383217.3:p.Thr1049Ile
ENST00000400370.8:c.2189C>T	ENSP00000383221.3:p.Thr730Ile
ENST00000418097.7:c.3284C>T	ENSP00000393343.2:p.Thr1095Ile
ENST00000448424.6:c.3245C>T	ENSP00000416738.2:p.Thr1082Ile
ENST00000634296.1:c.1257C>T
ENST00000634308.1:c.*580C>T	ENSP00000489234.1:n.*580C>T
ENST00000634620.1:n.4223C>T
ENST00000634810.1:n.2824C>T
ENST00000634844.1:c.3335C>T	ENSP00000489398.1:p.Thr1112Ile
NM_000053.3:c.3479C>T	NP_000044.2:p.Thr1160Ile
NM_001005918.2:c.2858C>T	NP_001005918.1:p.Thr953Ile
NM_001243182.1:c.3146C>T	NP_001230111.1:p.Thr1049Ile
XM_005266423.2:c.3383C>T	XP_005266480.1:p.Thr1128Ile
XM_005266424.3:c.3383C>T	XP_005266481.1:p.Thr1128Ile
XM_005266427.2:c.3245C>T	XP_005266484.1:p.Thr1082Ile
XM_005266428.1:c.3227C>T	XP_005266485.1:p.Thr1076Ile
XM_005266430.3:c.3479C>T	XP_005266487.1:p.Thr1160Ile
XM_005266431.2:c.3443C>T	XP_005266488.1:p.Thr1148Ile
XM_005266432.2:c.2993C>T	XP_005266489.1:p.Thr998Ile
XM_006719837.2:c.3383C>T	XP_006719900.1:p.Thr1128Ile
XM_006719838.1:c.1295C>T	XP_006719901.1:p.Thr432Ile
XM_006719839.1:c.1112C>T	XP_006719902.1:p.Thr371Ile
XM_011535117.1:c.3383C>T	XP_011533419.1:p.Thr1128Ile
XM_011535118.1:c.3344C>T	XP_011533420.1:p.Thr1115Ile
XM_011535119.1:c.3296C>T	XP_011533421.1:p.Thr1099Ile
XM_011535120.1:c.3065C>T	XP_011533422.1:p.Thr1022Ile
XM_011535121.1:c.2966C>T	XP_011533423.1:p.Thr989Ile
XM_011535122.1:c.2147C>T	XP_011533424.1:p.Thr716Ile
XR_941601.1:n.3698C>T
XR_941602.1:n.3698C>T
XR_941603.1:n.3698C>T
XR_941604.1:n.3698C>T
NM_001330578.1:c.3245C>T	NP_001317507.1:p.Thr1082Ile
NM_001330579.1:c.3227C>T	NP_001317508.1:p.Thr1076Ile
XM_005266424.4:c.3383C>T	XP_005266481.1:p.Thr1128Ile
XM_005266430.4:c.3479C>T	XP_005266487.1:p.Thr1160Ile
XM_005266431.4:c.3443C>T	XP_005266488.1:p.Thr1148Ile
XM_006719837.3:c.3383C>T	XP_006719900.1:p.Thr1128Ile
XM_011535117.3:c.3383C>T	XP_011533419.1:p.Thr1128Ile
XM_017020627.1:c.3383C>T	XP_016876116.1:p.Thr1128Ile
NM_000053.4:c.3479C>T MANE Select	NP_000044.2:p.Thr1160Ile
NM_001005918.3:c.2858C>T	NP_001005918.1:p.Thr953Ile
NM_001330579.2:c.3227C>T	NP_001317508.1:p.Thr1076Ile
NM_001243182.2:c.3146C>T	NP_001230111.1:p.Thr1049Ile
NM_001330578.2:c.3245C>T	NP_001317507.1:p.Thr1082Ile