Canonical Allele Identifier: CA388024266

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513272G>C (hg19) ; chr13:g.51939136G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939136G>C , CM000675.2:g.51939136G>C	GRCh38
NC_000013.10:g.52513272G>C , CM000675.1:g.52513272G>C	GRCh37
NC_000013.9:g.51411273G>C	NCBI36
NG_008806.1:g.77359C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1264C>G	ENSP00000489512.2:n.*1264C>G
ENST00000673864.2:c.*2358C>G	ENSP00000501045.2:n.*2358C>G
ENST00000674147.2:c.2993C>G	ENSP00000500964.2:p.Ala998Gly
ENST00000242839.10:c.3614C>G MANE Select	ENSP00000242839.5:p.Ala1205Gly
ENST00000344297.9:c.2993C>G	ENSP00000342559.5:p.Ala998Gly
ENST00000400366.6:c.3281C>G	ENSP00000383217.3:p.Ala1094Gly
ENST00000448424.7:c.3362C>G	ENSP00000416738.3:p.Ala1121Gly
ENST00000673696.1:n.855C>G
ENST00000673772.1:c.3380C>G	ENSP00000501168.1:p.Ala1127Gly
ENST00000673867.1:n.3753C>G
ENST00000673923.1:n.480C>G
ENST00000674147.1:c.2549C>G	ENSP00000500964.1:p.Ala850Gly
ENST00000242839.8:c.3614C>G	ENSP00000242839.4:p.Ala1205Gly
ENST00000344297.8:c.2993C>G	ENSP00000342559.5:p.Ala998Gly
ENST00000400366.5:c.3281C>G	ENSP00000383217.3:p.Ala1094Gly
ENST00000400370.8:c.2324C>G	ENSP00000383221.3:p.Ala775Gly
ENST00000418097.7:c.3419C>G	ENSP00000393343.2:p.Ala1140Gly
ENST00000448424.6:c.3380C>G	ENSP00000416738.2:p.Ala1127Gly
ENST00000634296.1:c.1392C>G
ENST00000634308.1:c.*715C>G	ENSP00000489234.1:n.*715C>G
ENST00000634620.1:n.4358C>G
ENST00000634810.1:n.2959C>G
ENST00000634844.1:c.3470C>G	ENSP00000489398.1:p.Ala1157Gly
NM_000053.3:c.3614C>G	NP_000044.2:p.Ala1205Gly
NM_001005918.2:c.2993C>G	NP_001005918.1:p.Ala998Gly
NM_001243182.1:c.3281C>G	NP_001230111.1:p.Ala1094Gly
XM_005266423.2:c.3518C>G	XP_005266480.1:p.Ala1173Gly
XM_005266424.3:c.3518C>G	XP_005266481.1:p.Ala1173Gly
XM_005266427.2:c.3380C>G	XP_005266484.1:p.Ala1127Gly
XM_005266428.1:c.3362C>G	XP_005266485.1:p.Ala1121Gly
XM_005266430.3:c.3614C>G	XP_005266487.1:p.Ala1205Gly
XM_005266431.2:c.3578C>G	XP_005266488.1:p.Ala1193Gly
XM_005266432.2:c.3128C>G	XP_005266489.1:p.Ala1043Gly
XM_006719837.2:c.3518C>G	XP_006719900.1:p.Ala1173Gly
XM_006719838.1:c.1430C>G	XP_006719901.1:p.Ala477Gly
XM_006719839.1:c.1247C>G	XP_006719902.1:p.Ala416Gly
XM_011535117.1:c.3518C>G	XP_011533419.1:p.Ala1173Gly
XM_011535118.1:c.3479C>G	XP_011533420.1:p.Ala1160Gly
XM_011535119.1:c.3431C>G	XP_011533421.1:p.Ala1144Gly
XM_011535120.1:c.3200C>G	XP_011533422.1:p.Ala1067Gly
XM_011535121.1:c.3101C>G	XP_011533423.1:p.Ala1034Gly
XM_011535122.1:c.2282C>G	XP_011533424.1:p.Ala761Gly
XR_941601.1:n.3833C>G
XR_941602.1:n.3833C>G
XR_941603.1:n.3833C>G
XR_941604.1:n.3833C>G
NM_001330578.1:c.3380C>G	NP_001317507.1:p.Ala1127Gly
NM_001330579.1:c.3362C>G	NP_001317508.1:p.Ala1121Gly
XM_005266424.4:c.3518C>G	XP_005266481.1:p.Ala1173Gly
XM_005266430.4:c.3614C>G	XP_005266487.1:p.Ala1205Gly
XM_005266431.4:c.3578C>G	XP_005266488.1:p.Ala1193Gly
XM_006719837.3:c.3518C>G	XP_006719900.1:p.Ala1173Gly
XM_011535117.3:c.3518C>G	XP_011533419.1:p.Ala1173Gly
XM_017020627.1:c.3518C>G	XP_016876116.1:p.Ala1173Gly
NM_000053.4:c.3614C>G MANE Select	NP_000044.2:p.Ala1205Gly
NM_001005918.3:c.2993C>G	NP_001005918.1:p.Ala998Gly
NM_001330579.2:c.3362C>G	NP_001317508.1:p.Ala1121Gly
NM_001243182.2:c.3281C>G	NP_001230111.1:p.Ala1094Gly
NM_001330578.2:c.3380C>G	NP_001317507.1:p.Ala1127Gly