Canonical Allele Identifier: CA270738

Gene: ATP7B

Linked Data

• dbSNP Id: rs137853279
• MyVariant Identifiers: chr13:g.52515247C>A (hg19) ; chr13:g.51941111C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941111C>A , CM000675.2:g.51941111C>A	GRCh38
NC_000013.10:g.52515247C>A , CM000675.1:g.52515247C>A	GRCh37
NC_000013.9:g.51413248C>A	NCBI36
NG_008806.1:g.75384G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1176G>T	ENSP00000489512.2:n.*1176G>T
ENST00000673864.2:c.*2270G>T	ENSP00000501045.2:n.*2270G>T
ENST00000674147.2:c.2905G>T	ENSP00000500964.2:p.Gly969Ter
ENST00000242839.10:c.3526G>T MANE Select	ENSP00000242839.5:p.Gly1176Ter
ENST00000344297.9:c.2905G>T	ENSP00000342559.5:p.Gly969Ter
ENST00000400366.6:c.3193G>T	ENSP00000383217.3:p.Gly1065Ter
ENST00000448424.7:c.3274G>T	ENSP00000416738.3:p.Gly1092Ter
ENST00000673772.1:c.3292G>T	ENSP00000501168.1:p.Gly1098Ter
ENST00000673867.1:n.3665G>T
ENST00000674126.1:n.3889G>T
ENST00000674147.1:c.2461G>T	ENSP00000500964.1:p.Gly821Ter
ENST00000242839.8:c.3526G>T	ENSP00000242839.4:p.Gly1176Ter
ENST00000344297.8:c.2905G>T	ENSP00000342559.5:p.Gly969Ter
ENST00000400366.5:c.3193G>T	ENSP00000383217.3:p.Gly1065Ter
ENST00000400370.8:c.2236G>T	ENSP00000383221.3:p.Gly746Ter
ENST00000418097.7:c.3331G>T	ENSP00000393343.2:p.Gly1111Ter
ENST00000448424.6:c.3292G>T	ENSP00000416738.2:p.Gly1098Ter
ENST00000634296.1:c.1304G>T
ENST00000634308.1:c.*627G>T	ENSP00000489234.1:n.*627G>T
ENST00000634620.1:n.4270G>T
ENST00000634810.1:n.2871G>T
ENST00000634844.1:c.3382G>T	ENSP00000489398.1:p.Gly1128Ter
NM_000053.3:c.3526G>T	NP_000044.2:p.Gly1176Ter
NM_001005918.2:c.2905G>T	NP_001005918.1:p.Gly969Ter
NM_001243182.1:c.3193G>T	NP_001230111.1:p.Gly1065Ter
XM_005266423.2:c.3430G>T	XP_005266480.1:p.Gly1144Ter
XM_005266424.3:c.3430G>T	XP_005266481.1:p.Gly1144Ter
XM_005266427.2:c.3292G>T	XP_005266484.1:p.Gly1098Ter
XM_005266428.1:c.3274G>T	XP_005266485.1:p.Gly1092Ter
XM_005266430.3:c.3526G>T	XP_005266487.1:p.Gly1176Ter
XM_005266431.2:c.3490G>T	XP_005266488.1:p.Gly1164Ter
XM_005266432.2:c.3040G>T	XP_005266489.1:p.Gly1014Ter
XM_006719837.2:c.3430G>T	XP_006719900.1:p.Gly1144Ter
XM_006719838.1:c.1342G>T	XP_006719901.1:p.Gly448Ter
XM_006719839.1:c.1159G>T	XP_006719902.1:p.Gly387Ter
XM_011535117.1:c.3430G>T	XP_011533419.1:p.Gly1144Ter
XM_011535118.1:c.3391G>T	XP_011533420.1:p.Gly1131Ter
XM_011535119.1:c.3343G>T	XP_011533421.1:p.Gly1115Ter
XM_011535120.1:c.3112G>T	XP_011533422.1:p.Gly1038Ter
XM_011535121.1:c.3013G>T	XP_011533423.1:p.Gly1005Ter
XM_011535122.1:c.2194G>T	XP_011533424.1:p.Gly732Ter
XR_941601.1:n.3745G>T
XR_941602.1:n.3745G>T
XR_941603.1:n.3745G>T
XR_941604.1:n.3745G>T
NM_001330578.1:c.3292G>T	NP_001317507.1:p.Gly1098Ter
NM_001330579.1:c.3274G>T	NP_001317508.1:p.Gly1092Ter
XM_005266424.4:c.3430G>T	XP_005266481.1:p.Gly1144Ter
XM_005266430.4:c.3526G>T	XP_005266487.1:p.Gly1176Ter
XM_005266431.4:c.3490G>T	XP_005266488.1:p.Gly1164Ter
XM_006719837.3:c.3430G>T	XP_006719900.1:p.Gly1144Ter
XM_011535117.3:c.3430G>T	XP_011533419.1:p.Gly1144Ter
XM_017020627.1:c.3430G>T	XP_016876116.1:p.Gly1144Ter
NM_000053.4:c.3526G>T MANE Select	NP_000044.2:p.Gly1176Ter
NM_001005918.3:c.2905G>T	NP_001005918.1:p.Gly969Ter
NM_001330579.2:c.3274G>T	NP_001317508.1:p.Gly1092Ter
NM_001243182.2:c.3193G>T	NP_001230111.1:p.Gly1065Ter
NM_001330578.2:c.3292G>T	NP_001317507.1:p.Gly1098Ter