Canonical Allele Identifier: CA483896520

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52539116C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51964980C>A , CM000675.2:g.51964980C>A	GRCh38
NC_000013.10:g.52539116C>A , CM000675.1:g.52539116C>A	GRCh37
NC_000013.9:g.51437117C>A	NCBI36
NG_008806.1:g.51515G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.1761G>T	ENSP00000489512.2:p.Thr587=
ENST00000673864.2:c.*505G>T	ENSP00000501045.2:n.*505G>T
ENST00000674147.2:c.1761G>T	ENSP00000500964.2:p.Thr587=
ENST00000242839.10:c.1761G>T MANE Select	ENSP00000242839.5:p.Thr587=
ENST00000344297.9:c.1761G>T	ENSP00000342559.5:p.Thr587=
ENST00000400366.6:c.1428G>T	ENSP00000383217.3:p.Thr476=
ENST00000448424.7:c.1761G>T	ENSP00000416738.3:p.Thr587=
ENST00000483772.2:n.517G>T
ENST00000673772.1:c.1761G>T	ENSP00000501168.1:p.Thr587=
ENST00000673864.1:c.955G>T	ENSP00000501045.1:n.955G>T
ENST00000674147.1:c.1317G>T	ENSP00000500964.1:p.Thr439=
ENST00000242839.8:c.1761G>T	ENSP00000242839.4:p.Thr587=
ENST00000344297.8:c.1761G>T	ENSP00000342559.5:p.Thr587=
ENST00000400366.5:c.1428G>T	ENSP00000383217.3:p.Thr476=
ENST00000400370.8:c.1285+8955G>T	ENSP00000383221.3:n.1285+8955G>T
ENST00000418097.7:c.1761G>T	ENSP00000393343.2:p.Thr587=
ENST00000448424.6:c.1761G>T	ENSP00000416738.2:p.Thr587=
ENST00000482841.6:n.1664+5512G>T
ENST00000483772.1:n.517G>T
ENST00000634308.1:c.1761G>T	ENSP00000489234.1:p.Thr587=
ENST00000634620.1:n.253G>T
ENST00000634844.1:c.1761G>T	ENSP00000489398.1:p.Thr587=
ENST00000635406.1:n.212-18502G>T
NM_000053.3:c.1761G>T	NP_000044.2:p.Thr587=
NM_001005918.2:c.1761G>T	NP_001005918.1:p.Thr587=
NM_001243182.1:c.1428G>T	NP_001230111.1:p.Thr476=
XM_005266423.2:c.1665G>T	XP_005266480.1:p.Thr555=
XM_005266424.3:c.1665G>T	XP_005266481.1:p.Thr555=
XM_005266427.2:c.1761G>T	XP_005266484.1:p.Thr587=
XM_005266428.1:c.1761G>T	XP_005266485.1:p.Thr587=
XM_005266430.3:c.1761G>T	XP_005266487.1:p.Thr587=
XM_005266431.2:c.1725G>T	XP_005266488.1:p.Thr575=
XM_005266432.2:c.1761G>T	XP_005266489.1:p.Thr587=
XM_006719837.2:c.1665G>T	XP_006719900.1:p.Thr555=
XM_011535117.1:c.1665G>T	XP_011533419.1:p.Thr555=
XM_011535118.1:c.1761G>T	XP_011533420.1:p.Thr587=
XM_011535119.1:c.1761G>T	XP_011533421.1:p.Thr587=
XM_011535120.1:c.1707+3464G>T	XP_011533422.1:n.1707+3464G>T
XM_011535121.1:c.1761G>T	XP_011533423.1:p.Thr587=
XM_011535122.1:c.429G>T	XP_011533424.1:p.Thr143=
XR_941601.1:n.1980G>T
XR_941602.1:n.1980G>T
XR_941603.1:n.1980G>T
XR_941604.1:n.1980G>T
NM_001330578.1:c.1761G>T	NP_001317507.1:p.Thr587=
NM_001330579.1:c.1761G>T	NP_001317508.1:p.Thr587=
XM_005266424.4:c.1665G>T	XP_005266481.1:p.Thr555=
XM_005266430.4:c.1761G>T	XP_005266487.1:p.Thr587=
XM_005266431.4:c.1725G>T	XP_005266488.1:p.Thr575=
XM_006719837.3:c.1665G>T	XP_006719900.1:p.Thr555=
XM_011535117.3:c.1665G>T	XP_011533419.1:p.Thr555=
XM_017020627.1:c.1665G>T	XP_016876116.1:p.Thr555=
NM_000053.4:c.1761G>T MANE Select	NP_000044.2:p.Thr587=
NM_001005918.3:c.1761G>T	NP_001005918.1:p.Thr587=
NM_001330579.2:c.1761G>T	NP_001317508.1:p.Thr587=
NM_001243182.2:c.1428G>T	NP_001230111.1:p.Thr476=
NM_001330578.2:c.1761G>T	NP_001317507.1:p.Thr587=