Canonical Allele Identifier: CA483894762

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518401A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944265A>T , CM000675.2:g.51944265A>T	GRCh38
NC_000013.10:g.52518401A>T , CM000675.1:g.52518401A>T	GRCh37
NC_000013.9:g.51416402A>T	NCBI36
NG_008806.1:g.72230T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1711T>A	ENSP00000489512.2:n.*894-1711T>A
ENST00000673864.2:c.*1831T>A	ENSP00000501045.2:n.*1831T>A
ENST00000674147.2:c.2466T>A	ENSP00000500964.2:p.Thr822=
ENST00000242839.10:c.3087T>A MANE Select	ENSP00000242839.5:p.Thr1029=
ENST00000344297.9:c.2466T>A	ENSP00000342559.5:p.Thr822=
ENST00000400366.6:c.2754T>A	ENSP00000383217.3:p.Thr918=
ENST00000448424.7:c.2835T>A	ENSP00000416738.3:p.Thr945=
ENST00000673772.1:c.2853T>A	ENSP00000501168.1:p.Thr951=
ENST00000673867.1:n.3226T>A
ENST00000674126.1:n.3450T>A
ENST00000674147.1:c.2022T>A	ENSP00000500964.1:p.Thr674=
ENST00000242839.8:c.3087T>A	ENSP00000242839.4:p.Thr1029=
ENST00000344297.8:c.2466T>A	ENSP00000342559.5:p.Thr822=
ENST00000400366.5:c.2754T>A	ENSP00000383217.3:p.Thr918=
ENST00000400370.8:c.1797T>A	ENSP00000383221.3:p.Thr599=
ENST00000418097.7:c.2892T>A	ENSP00000393343.2:p.Thr964=
ENST00000448424.6:c.2853T>A	ENSP00000416738.2:p.Thr951=
ENST00000466629.1:n.307T>A
ENST00000634296.1:c.1022-1711T>A
ENST00000634308.1:c.*188T>A	ENSP00000489234.1:n.*188T>A
ENST00000634620.1:n.3831T>A
ENST00000634810.1:n.2432T>A
ENST00000634844.1:c.2943T>A	ENSP00000489398.1:p.Thr981=
ENST00000635406.1:n.433T>A
NM_000053.3:c.3087T>A	NP_000044.2:p.Thr1029=
NM_001005918.2:c.2466T>A	NP_001005918.1:p.Thr822=
NM_001243182.1:c.2754T>A	NP_001230111.1:p.Thr918=
XM_005266423.2:c.2991T>A	XP_005266480.1:p.Thr997=
XM_005266424.3:c.2991T>A	XP_005266481.1:p.Thr997=
XM_005266427.2:c.2853T>A	XP_005266484.1:p.Thr951=
XM_005266428.1:c.2835T>A	XP_005266485.1:p.Thr945=
XM_005266430.3:c.3087T>A	XP_005266487.1:p.Thr1029=
XM_005266431.2:c.3051T>A	XP_005266488.1:p.Thr1017=
XM_005266432.2:c.2601T>A	XP_005266489.1:p.Thr867=
XM_006719837.2:c.2991T>A	XP_006719900.1:p.Thr997=
XM_006719838.1:c.903T>A	XP_006719901.1:p.Thr301=
XM_006719839.1:c.877-1711T>A	XP_006719902.1:n.877-1711T>A
XM_011535117.1:c.2991T>A	XP_011533419.1:p.Thr997=
XM_011535118.1:c.2952T>A	XP_011533420.1:p.Thr984=
XM_011535119.1:c.3061-1711T>A	XP_011533421.1:n.3061-1711T>A
XM_011535120.1:c.2673T>A	XP_011533422.1:p.Thr891=
XM_011535121.1:c.2731-1711T>A	XP_011533423.1:n.2731-1711T>A
XM_011535122.1:c.1755T>A	XP_011533424.1:p.Thr585=
XR_941601.1:n.3306T>A
XR_941602.1:n.3306T>A
XR_941603.1:n.3306T>A
XR_941604.1:n.3306T>A
NM_001330578.1:c.2853T>A	NP_001317507.1:p.Thr951=
NM_001330579.1:c.2835T>A	NP_001317508.1:p.Thr945=
XM_005266424.4:c.2991T>A	XP_005266481.1:p.Thr997=
XM_005266430.4:c.3087T>A	XP_005266487.1:p.Thr1029=
XM_005266431.4:c.3051T>A	XP_005266488.1:p.Thr1017=
XM_006719837.3:c.2991T>A	XP_006719900.1:p.Thr997=
XM_011535117.3:c.2991T>A	XP_011533419.1:p.Thr997=
XM_017020627.1:c.2991T>A	XP_016876116.1:p.Thr997=
NM_000053.4:c.3087T>A MANE Select	NP_000044.2:p.Thr1029=
NM_001005918.3:c.2466T>A	NP_001005918.1:p.Thr822=
NM_001330579.2:c.2835T>A	NP_001317508.1:p.Thr945=
NM_001243182.2:c.2754T>A	NP_001230111.1:p.Thr918=
NM_001330578.2:c.2853T>A	NP_001317507.1:p.Thr951=