Canonical Allele Identifier: CA484024433

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52524260A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950124A>T , CM000675.2:g.51950124A>T	GRCh38
NC_000013.10:g.52524260A>T , CM000675.1:g.52524260A>T	GRCh37
NC_000013.9:g.51422261A>T	NCBI36
NG_008806.1:g.66371T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*446T>A	ENSP00000489512.2:n.*446T>A
ENST00000673864.2:c.*1357T>A	ENSP00000501045.2:n.*1357T>A
ENST00000674147.2:c.2127T>A	ENSP00000500964.2:p.Thr709=
ENST00000242839.10:c.2613T>A MANE Select	ENSP00000242839.5:p.Thr871=
ENST00000344297.9:c.2127T>A	ENSP00000342559.5:p.Thr709=
ENST00000400366.6:c.2280T>A	ENSP00000383217.3:p.Thr760=
ENST00000448424.7:c.2361T>A	ENSP00000416738.3:p.Thr787=
ENST00000673772.1:c.2379T>A	ENSP00000501168.1:p.Thr793=
ENST00000674147.1:c.1683T>A	ENSP00000500964.1:p.Thr561=
ENST00000242839.8:c.2613T>A	ENSP00000242839.4:p.Thr871=
ENST00000344297.8:c.2127T>A	ENSP00000342559.5:p.Thr709=
ENST00000400366.5:c.2280T>A	ENSP00000383217.3:p.Thr760=
ENST00000400370.8:c.1323T>A	ENSP00000383221.3:p.Thr441=
ENST00000418097.7:c.2613T>A	ENSP00000393343.2:p.Thr871=
ENST00000448424.6:c.2379T>A	ENSP00000416738.2:p.Thr793=
ENST00000634296.1:c.574T>A
ENST00000634308.1:c.2379T>A	ENSP00000489234.1:p.Thr793=
ENST00000634620.1:n.3411T>A
ENST00000634810.1:n.1958T>A
ENST00000634844.1:c.2469T>A	ENSP00000489398.1:p.Thr823=
ENST00000635406.1:n.212-3646T>A
NM_000053.3:c.2613T>A	NP_000044.2:p.Thr871=
NM_001005918.2:c.2127T>A	NP_001005918.1:p.Thr709=
NM_001243182.1:c.2280T>A	NP_001230111.1:p.Thr760=
XM_005266423.2:c.2517T>A	XP_005266480.1:p.Thr839=
XM_005266424.3:c.2517T>A	XP_005266481.1:p.Thr839=
XM_005266427.2:c.2379T>A	XP_005266484.1:p.Thr793=
XM_005266428.1:c.2361T>A	XP_005266485.1:p.Thr787=
XM_005266430.3:c.2613T>A	XP_005266487.1:p.Thr871=
XM_005266431.2:c.2577T>A	XP_005266488.1:p.Thr859=
XM_005266432.2:c.2127T>A	XP_005266489.1:p.Thr709=
XM_006719837.2:c.2517T>A	XP_006719900.1:p.Thr839=
XM_006719838.1:c.429T>A	XP_006719901.1:p.Thr143=
XM_006719839.1:c.429T>A	XP_006719902.1:p.Thr143=
XM_011535117.1:c.2517T>A	XP_011533419.1:p.Thr839=
XM_011535118.1:c.2613T>A	XP_011533420.1:p.Thr871=
XM_011535119.1:c.2613T>A	XP_011533421.1:p.Thr871=
XM_011535120.1:c.2199T>A	XP_011533422.1:p.Thr733=
XM_011535121.1:c.2613T>A	XP_011533423.1:p.Thr871=
XM_011535122.1:c.1281T>A	XP_011533424.1:p.Thr427=
XR_941601.1:n.2832T>A
XR_941602.1:n.2832T>A
XR_941603.1:n.2832T>A
XR_941604.1:n.2832T>A
NM_001330578.1:c.2379T>A	NP_001317507.1:p.Thr793=
NM_001330579.1:c.2361T>A	NP_001317508.1:p.Thr787=
XM_005266424.4:c.2517T>A	XP_005266481.1:p.Thr839=
XM_005266430.4:c.2613T>A	XP_005266487.1:p.Thr871=
XM_005266431.4:c.2577T>A	XP_005266488.1:p.Thr859=
XM_006719837.3:c.2517T>A	XP_006719900.1:p.Thr839=
XM_011535117.3:c.2517T>A	XP_011533419.1:p.Thr839=
XM_017020627.1:c.2517T>A	XP_016876116.1:p.Thr839=
NM_000053.4:c.2613T>A MANE Select	NP_000044.2:p.Thr871=
NM_001005918.3:c.2127T>A	NP_001005918.1:p.Thr709=
NM_001330579.2:c.2361T>A	NP_001317508.1:p.Thr787=
NM_001243182.2:c.2280T>A	NP_001230111.1:p.Thr760=
NM_001330578.2:c.2379T>A	NP_001317507.1:p.Thr793=