Canonical Allele Identifier: CA483893978

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515287A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941151A>G , CM000675.2:g.51941151A>G	GRCh38
NC_000013.10:g.52515287A>G , CM000675.1:g.52515287A>G	GRCh37
NC_000013.9:g.51413288A>G	NCBI36
NG_008806.1:g.75344T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1136T>C	ENSP00000489512.2:n.*1136T>C
ENST00000673864.2:c.*2230T>C	ENSP00000501045.2:n.*2230T>C
ENST00000674147.2:c.2865T>C	ENSP00000500964.2:p.Ser955=
ENST00000242839.10:c.3486T>C MANE Select	ENSP00000242839.5:p.Ser1162=
ENST00000344297.9:c.2865T>C	ENSP00000342559.5:p.Ser955=
ENST00000400366.6:c.3153T>C	ENSP00000383217.3:p.Ser1051=
ENST00000448424.7:c.3234T>C	ENSP00000416738.3:p.Ser1078=
ENST00000673772.1:c.3252T>C	ENSP00000501168.1:p.Ser1084=
ENST00000673867.1:n.3625T>C
ENST00000674126.1:n.3849T>C
ENST00000674147.1:c.2421T>C	ENSP00000500964.1:p.Ser807=
ENST00000242839.8:c.3486T>C	ENSP00000242839.4:p.Ser1162=
ENST00000344297.8:c.2865T>C	ENSP00000342559.5:p.Ser955=
ENST00000400366.5:c.3153T>C	ENSP00000383217.3:p.Ser1051=
ENST00000400370.8:c.2196T>C	ENSP00000383221.3:p.Ser732=
ENST00000418097.7:c.3291T>C	ENSP00000393343.2:p.Ser1097=
ENST00000448424.6:c.3252T>C	ENSP00000416738.2:p.Ser1084=
ENST00000634296.1:c.1264T>C
ENST00000634308.1:c.*587T>C	ENSP00000489234.1:n.*587T>C
ENST00000634620.1:n.4230T>C
ENST00000634810.1:n.2831T>C
ENST00000634844.1:c.3342T>C	ENSP00000489398.1:p.Ser1114=
NM_000053.3:c.3486T>C	NP_000044.2:p.Ser1162=
NM_001005918.2:c.2865T>C	NP_001005918.1:p.Ser955=
NM_001243182.1:c.3153T>C	NP_001230111.1:p.Ser1051=
XM_005266423.2:c.3390T>C	XP_005266480.1:p.Ser1130=
XM_005266424.3:c.3390T>C	XP_005266481.1:p.Ser1130=
XM_005266427.2:c.3252T>C	XP_005266484.1:p.Ser1084=
XM_005266428.1:c.3234T>C	XP_005266485.1:p.Ser1078=
XM_005266430.3:c.3486T>C	XP_005266487.1:p.Ser1162=
XM_005266431.2:c.3450T>C	XP_005266488.1:p.Ser1150=
XM_005266432.2:c.3000T>C	XP_005266489.1:p.Ser1000=
XM_006719837.2:c.3390T>C	XP_006719900.1:p.Ser1130=
XM_006719838.1:c.1302T>C	XP_006719901.1:p.Ser434=
XM_006719839.1:c.1119T>C	XP_006719902.1:p.Ser373=
XM_011535117.1:c.3390T>C	XP_011533419.1:p.Ser1130=
XM_011535118.1:c.3351T>C	XP_011533420.1:p.Ser1117=
XM_011535119.1:c.3303T>C	XP_011533421.1:p.Ser1101=
XM_011535120.1:c.3072T>C	XP_011533422.1:p.Ser1024=
XM_011535121.1:c.2973T>C	XP_011533423.1:p.Ser991=
XM_011535122.1:c.2154T>C	XP_011533424.1:p.Ser718=
XR_941601.1:n.3705T>C
XR_941602.1:n.3705T>C
XR_941603.1:n.3705T>C
XR_941604.1:n.3705T>C
NM_001330578.1:c.3252T>C	NP_001317507.1:p.Ser1084=
NM_001330579.1:c.3234T>C	NP_001317508.1:p.Ser1078=
XM_005266424.4:c.3390T>C	XP_005266481.1:p.Ser1130=
XM_005266430.4:c.3486T>C	XP_005266487.1:p.Ser1162=
XM_005266431.4:c.3450T>C	XP_005266488.1:p.Ser1150=
XM_006719837.3:c.3390T>C	XP_006719900.1:p.Ser1130=
XM_011535117.3:c.3390T>C	XP_011533419.1:p.Ser1130=
XM_017020627.1:c.3390T>C	XP_016876116.1:p.Ser1130=
NM_000053.4:c.3486T>C MANE Select	NP_000044.2:p.Ser1162=
NM_001005918.3:c.2865T>C	NP_001005918.1:p.Ser955=
NM_001330579.2:c.3234T>C	NP_001317508.1:p.Ser1078=
NM_001243182.2:c.3153T>C	NP_001230111.1:p.Ser1051=
NM_001330578.2:c.3252T>C	NP_001317507.1:p.Ser1084=