Canonical Allele Identifier: CA388026145

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51941119-T-A
• MyVariant Identifiers: chr13:g.52515255T>A (hg19) ; chr13:g.51941119T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941119T>A , CM000675.2:g.51941119T>A	GRCh38
NC_000013.10:g.52515255T>A , CM000675.1:g.52515255T>A	GRCh37
NC_000013.9:g.51413256T>A	NCBI36
NG_008806.1:g.75376A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1168A>T	ENSP00000489512.2:n.*1168A>T
ENST00000673864.2:c.*2262A>T	ENSP00000501045.2:n.*2262A>T
ENST00000674147.2:c.2897A>T	ENSP00000500964.2:p.Glu966Val
ENST00000242839.10:c.3518A>T MANE Select	ENSP00000242839.5:p.Glu1173Val
ENST00000344297.9:c.2897A>T	ENSP00000342559.5:p.Glu966Val
ENST00000400366.6:c.3185A>T	ENSP00000383217.3:p.Glu1062Val
ENST00000448424.7:c.3266A>T	ENSP00000416738.3:p.Glu1089Val
ENST00000673772.1:c.3284A>T	ENSP00000501168.1:p.Glu1095Val
ENST00000673867.1:n.3657A>T
ENST00000674126.1:n.3881A>T
ENST00000674147.1:c.2453A>T	ENSP00000500964.1:p.Glu818Val
ENST00000242839.8:c.3518A>T	ENSP00000242839.4:p.Glu1173Val
ENST00000344297.8:c.2897A>T	ENSP00000342559.5:p.Glu966Val
ENST00000400366.5:c.3185A>T	ENSP00000383217.3:p.Glu1062Val
ENST00000400370.8:c.2228A>T	ENSP00000383221.3:p.Glu743Val
ENST00000418097.7:c.3323A>T	ENSP00000393343.2:p.Glu1108Val
ENST00000448424.6:c.3284A>T	ENSP00000416738.2:p.Glu1095Val
ENST00000634296.1:c.1296A>T
ENST00000634308.1:c.*619A>T	ENSP00000489234.1:n.*619A>T
ENST00000634620.1:n.4262A>T
ENST00000634810.1:n.2863A>T
ENST00000634844.1:c.3374A>T	ENSP00000489398.1:p.Glu1125Val
NM_000053.3:c.3518A>T	NP_000044.2:p.Glu1173Val
NM_001005918.2:c.2897A>T	NP_001005918.1:p.Glu966Val
NM_001243182.1:c.3185A>T	NP_001230111.1:p.Glu1062Val
XM_005266423.2:c.3422A>T	XP_005266480.1:p.Glu1141Val
XM_005266424.3:c.3422A>T	XP_005266481.1:p.Glu1141Val
XM_005266427.2:c.3284A>T	XP_005266484.1:p.Glu1095Val
XM_005266428.1:c.3266A>T	XP_005266485.1:p.Glu1089Val
XM_005266430.3:c.3518A>T	XP_005266487.1:p.Glu1173Val
XM_005266431.2:c.3482A>T	XP_005266488.1:p.Glu1161Val
XM_005266432.2:c.3032A>T	XP_005266489.1:p.Glu1011Val
XM_006719837.2:c.3422A>T	XP_006719900.1:p.Glu1141Val
XM_006719838.1:c.1334A>T	XP_006719901.1:p.Glu445Val
XM_006719839.1:c.1151A>T	XP_006719902.1:p.Glu384Val
XM_011535117.1:c.3422A>T	XP_011533419.1:p.Glu1141Val
XM_011535118.1:c.3383A>T	XP_011533420.1:p.Glu1128Val
XM_011535119.1:c.3335A>T	XP_011533421.1:p.Glu1112Val
XM_011535120.1:c.3104A>T	XP_011533422.1:p.Glu1035Val
XM_011535121.1:c.3005A>T	XP_011533423.1:p.Glu1002Val
XM_011535122.1:c.2186A>T	XP_011533424.1:p.Glu729Val
XR_941601.1:n.3737A>T
XR_941602.1:n.3737A>T
XR_941603.1:n.3737A>T
XR_941604.1:n.3737A>T
NM_001330578.1:c.3284A>T	NP_001317507.1:p.Glu1095Val
NM_001330579.1:c.3266A>T	NP_001317508.1:p.Glu1089Val
XM_005266424.4:c.3422A>T	XP_005266481.1:p.Glu1141Val
XM_005266430.4:c.3518A>T	XP_005266487.1:p.Glu1173Val
XM_005266431.4:c.3482A>T	XP_005266488.1:p.Glu1161Val
XM_006719837.3:c.3422A>T	XP_006719900.1:p.Glu1141Val
XM_011535117.3:c.3422A>T	XP_011533419.1:p.Glu1141Val
XM_017020627.1:c.3422A>T	XP_016876116.1:p.Glu1141Val
NM_000053.4:c.3518A>T MANE Select	NP_000044.2:p.Glu1173Val
NM_001005918.3:c.2897A>T	NP_001005918.1:p.Glu966Val
NM_001330579.2:c.3266A>T	NP_001317508.1:p.Glu1089Val
NM_001243182.2:c.3185A>T	NP_001230111.1:p.Glu1062Val
NM_001330578.2:c.3284A>T	NP_001317507.1:p.Glu1095Val