Canonical Allele Identifier: CA388026069

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515246C>A (hg19) ; chr13:g.51941110C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941110C>A , CM000675.2:g.51941110C>A	GRCh38
NC_000013.10:g.52515246C>A , CM000675.1:g.52515246C>A	GRCh37
NC_000013.9:g.51413247C>A	NCBI36
NG_008806.1:g.75385G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1177G>T	ENSP00000489512.2:n.*1177G>T
ENST00000673864.2:c.*2271G>T	ENSP00000501045.2:n.*2271G>T
ENST00000674147.2:c.2906G>T	ENSP00000500964.2:p.Gly969Val
ENST00000242839.10:c.3527G>T MANE Select	ENSP00000242839.5:p.Gly1176Val
ENST00000344297.9:c.2906G>T	ENSP00000342559.5:p.Gly969Val
ENST00000400366.6:c.3194G>T	ENSP00000383217.3:p.Gly1065Val
ENST00000448424.7:c.3275G>T	ENSP00000416738.3:p.Gly1092Val
ENST00000673772.1:c.3293G>T	ENSP00000501168.1:p.Gly1098Val
ENST00000673867.1:n.3666G>T
ENST00000674126.1:n.3890G>T
ENST00000674147.1:c.2462G>T	ENSP00000500964.1:p.Gly821Val
ENST00000242839.8:c.3527G>T	ENSP00000242839.4:p.Gly1176Val
ENST00000344297.8:c.2906G>T	ENSP00000342559.5:p.Gly969Val
ENST00000400366.5:c.3194G>T	ENSP00000383217.3:p.Gly1065Val
ENST00000400370.8:c.2237G>T	ENSP00000383221.3:p.Gly746Val
ENST00000418097.7:c.3332G>T	ENSP00000393343.2:p.Gly1111Val
ENST00000448424.6:c.3293G>T	ENSP00000416738.2:p.Gly1098Val
ENST00000634296.1:c.1305G>T
ENST00000634308.1:c.*628G>T	ENSP00000489234.1:n.*628G>T
ENST00000634620.1:n.4271G>T
ENST00000634810.1:n.2872G>T
ENST00000634844.1:c.3383G>T	ENSP00000489398.1:p.Gly1128Val
NM_000053.3:c.3527G>T	NP_000044.2:p.Gly1176Val
NM_001005918.2:c.2906G>T	NP_001005918.1:p.Gly969Val
NM_001243182.1:c.3194G>T	NP_001230111.1:p.Gly1065Val
XM_005266423.2:c.3431G>T	XP_005266480.1:p.Gly1144Val
XM_005266424.3:c.3431G>T	XP_005266481.1:p.Gly1144Val
XM_005266427.2:c.3293G>T	XP_005266484.1:p.Gly1098Val
XM_005266428.1:c.3275G>T	XP_005266485.1:p.Gly1092Val
XM_005266430.3:c.3527G>T	XP_005266487.1:p.Gly1176Val
XM_005266431.2:c.3491G>T	XP_005266488.1:p.Gly1164Val
XM_005266432.2:c.3041G>T	XP_005266489.1:p.Gly1014Val
XM_006719837.2:c.3431G>T	XP_006719900.1:p.Gly1144Val
XM_006719838.1:c.1343G>T	XP_006719901.1:p.Gly448Val
XM_006719839.1:c.1160G>T	XP_006719902.1:p.Gly387Val
XM_011535117.1:c.3431G>T	XP_011533419.1:p.Gly1144Val
XM_011535118.1:c.3392G>T	XP_011533420.1:p.Gly1131Val
XM_011535119.1:c.3344G>T	XP_011533421.1:p.Gly1115Val
XM_011535120.1:c.3113G>T	XP_011533422.1:p.Gly1038Val
XM_011535121.1:c.3014G>T	XP_011533423.1:p.Gly1005Val
XM_011535122.1:c.2195G>T	XP_011533424.1:p.Gly732Val
XR_941601.1:n.3746G>T
XR_941602.1:n.3746G>T
XR_941603.1:n.3746G>T
XR_941604.1:n.3746G>T
NM_001330578.1:c.3293G>T	NP_001317507.1:p.Gly1098Val
NM_001330579.1:c.3275G>T	NP_001317508.1:p.Gly1092Val
XM_005266424.4:c.3431G>T	XP_005266481.1:p.Gly1144Val
XM_005266430.4:c.3527G>T	XP_005266487.1:p.Gly1176Val
XM_005266431.4:c.3491G>T	XP_005266488.1:p.Gly1164Val
XM_006719837.3:c.3431G>T	XP_006719900.1:p.Gly1144Val
XM_011535117.3:c.3431G>T	XP_011533419.1:p.Gly1144Val
XM_017020627.1:c.3431G>T	XP_016876116.1:p.Gly1144Val
NM_000053.4:c.3527G>T MANE Select	NP_000044.2:p.Gly1176Val
NM_001005918.3:c.2906G>T	NP_001005918.1:p.Gly969Val
NM_001330579.2:c.3275G>T	NP_001317508.1:p.Gly1092Val
NM_001243182.2:c.3194G>T	NP_001230111.1:p.Gly1065Val
NM_001330578.2:c.3293G>T	NP_001317507.1:p.Gly1098Val