Canonical Allele Identifier: CA388026063

Gene: ATP7B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1177G>C	ENSP00000489512.2:n.*1177G>C
ENST00000673864.2:c.*2271G>C	ENSP00000501045.2:n.*2271G>C
ENST00000674147.2:c.2906G>C	ENSP00000500964.2:p.Gly969Ala
ENST00000242839.10:c.3527G>C MANE Select	ENSP00000242839.5:p.Gly1176Ala
ENST00000344297.9:c.2906G>C	ENSP00000342559.5:p.Gly969Ala
ENST00000400366.6:c.3194G>C	ENSP00000383217.3:p.Gly1065Ala
ENST00000448424.7:c.3275G>C	ENSP00000416738.3:p.Gly1092Ala
ENST00000673772.1:c.3293G>C	ENSP00000501168.1:p.Gly1098Ala
ENST00000673867.1:n.3666G>C
ENST00000674126.1:n.3890G>C
ENST00000674147.1:c.2462G>C	ENSP00000500964.1:p.Gly821Ala
ENST00000242839.8:c.3527G>C	ENSP00000242839.4:p.Gly1176Ala
ENST00000344297.8:c.2906G>C	ENSP00000342559.5:p.Gly969Ala
ENST00000400366.5:c.3194G>C	ENSP00000383217.3:p.Gly1065Ala
ENST00000400370.8:c.2237G>C	ENSP00000383221.3:p.Gly746Ala
ENST00000418097.7:c.3332G>C	ENSP00000393343.2:p.Gly1111Ala
ENST00000448424.6:c.3293G>C	ENSP00000416738.2:p.Gly1098Ala
ENST00000634296.1:c.1305G>C
ENST00000634308.1:c.*628G>C	ENSP00000489234.1:n.*628G>C
ENST00000634620.1:n.4271G>C
ENST00000634810.1:n.2872G>C
ENST00000634844.1:c.3383G>C	ENSP00000489398.1:p.Gly1128Ala
NM_000053.3:c.3527G>C	NP_000044.2:p.Gly1176Ala
NM_001005918.2:c.2906G>C	NP_001005918.1:p.Gly969Ala
NM_001243182.1:c.3194G>C	NP_001230111.1:p.Gly1065Ala
XM_005266423.2:c.3431G>C	XP_005266480.1:p.Gly1144Ala
XM_005266424.3:c.3431G>C	XP_005266481.1:p.Gly1144Ala
XM_005266427.2:c.3293G>C	XP_005266484.1:p.Gly1098Ala
XM_005266428.1:c.3275G>C	XP_005266485.1:p.Gly1092Ala
XM_005266430.3:c.3527G>C	XP_005266487.1:p.Gly1176Ala
XM_005266431.2:c.3491G>C	XP_005266488.1:p.Gly1164Ala
XM_005266432.2:c.3041G>C	XP_005266489.1:p.Gly1014Ala
XM_006719837.2:c.3431G>C	XP_006719900.1:p.Gly1144Ala
XM_006719838.1:c.1343G>C	XP_006719901.1:p.Gly448Ala
XM_006719839.1:c.1160G>C	XP_006719902.1:p.Gly387Ala
XM_011535117.1:c.3431G>C	XP_011533419.1:p.Gly1144Ala
XM_011535118.1:c.3392G>C	XP_011533420.1:p.Gly1131Ala
XM_011535119.1:c.3344G>C	XP_011533421.1:p.Gly1115Ala
XM_011535120.1:c.3113G>C	XP_011533422.1:p.Gly1038Ala
XM_011535121.1:c.3014G>C	XP_011533423.1:p.Gly1005Ala
XM_011535122.1:c.2195G>C	XP_011533424.1:p.Gly732Ala
XR_941601.1:n.3746G>C
XR_941602.1:n.3746G>C
XR_941603.1:n.3746G>C
XR_941604.1:n.3746G>C
NM_001330578.1:c.3293G>C	NP_001317507.1:p.Gly1098Ala
NM_001330579.1:c.3275G>C	NP_001317508.1:p.Gly1092Ala
XM_005266424.4:c.3431G>C	XP_005266481.1:p.Gly1144Ala
XM_005266430.4:c.3527G>C	XP_005266487.1:p.Gly1176Ala
XM_005266431.4:c.3491G>C	XP_005266488.1:p.Gly1164Ala
XM_006719837.3:c.3431G>C	XP_006719900.1:p.Gly1144Ala
XM_011535117.3:c.3431G>C	XP_011533419.1:p.Gly1144Ala
XM_017020627.1:c.3431G>C	XP_016876116.1:p.Gly1144Ala
NM_000053.4:c.3527G>C MANE Select	NP_000044.2:p.Gly1176Ala
NM_001005918.3:c.2906G>C	NP_001005918.1:p.Gly969Ala
NM_001330579.2:c.3275G>C	NP_001317508.1:p.Gly1092Ala
NM_001243182.2:c.3194G>C	NP_001230111.1:p.Gly1065Ala
NM_001330578.2:c.3293G>C	NP_001317507.1:p.Gly1098Ala