Canonical Allele Identifier: CA2091563850

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944164G= , CM000675.2:g.51944164G=	GRCh38
NC_000013.10:g.52518300G= , CM000675.1:g.52518300G=	GRCh37
NC_000013.9:g.51416301G=	NCBI36
NG_008806.1:g.72331C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1610C=	ENSP00000489512.2:n.*894-1610C=
ENST00000673864.2:c.*1932C=	ENSP00000501045.2:n.*1932C=
ENST00000674147.2:c.2567C=	ENSP00000500964.2:p.Ala856=
ENST00000242839.10:c.3188C= MANE Select	ENSP00000242839.5:p.Ala1063=
ENST00000344297.9:c.2567C=	ENSP00000342559.5:p.Ala856=
ENST00000400366.6:c.2855C=	ENSP00000383217.3:p.Ala952=
ENST00000448424.7:c.2936C=	ENSP00000416738.3:p.Ala979=
ENST00000673772.1:c.2954C=	ENSP00000501168.1:p.Ala985=
ENST00000673867.1:n.3327C=
ENST00000674126.1:n.3551C=
ENST00000674147.1:c.2123C=	ENSP00000500964.1:p.Ala708=
ENST00000242839.8:c.3188C=	ENSP00000242839.4:p.Ala1063=
ENST00000344297.8:c.2567C=	ENSP00000342559.5:p.Ala856=
ENST00000400366.5:c.2855C=	ENSP00000383217.3:p.Ala952=
ENST00000400370.8:c.1898C=	ENSP00000383221.3:p.Ala633=
ENST00000418097.7:c.2993C=	ENSP00000393343.2:p.Ala998=
ENST00000448424.6:c.2954C=	ENSP00000416738.2:p.Ala985=
ENST00000466629.1:n.408C=
ENST00000634296.1:c.1022-1610C=
ENST00000634308.1:c.*289C=	ENSP00000489234.1:n.*289C=
ENST00000634620.1:n.3932C=
ENST00000634810.1:n.2533C=
ENST00000634844.1:c.3044C=	ENSP00000489398.1:p.Ala1015=
NM_000053.3:c.3188C=	NP_000044.2:p.Ala1063=
NM_001005918.2:c.2567C=	NP_001005918.1:p.Ala856=
NM_001243182.1:c.2855C=	NP_001230111.1:p.Ala952=
XM_005266423.2:c.3092C=	XP_005266480.1:p.Ala1031=
XM_005266424.3:c.3092C=	XP_005266481.1:p.Ala1031=
XM_005266427.2:c.2954C=	XP_005266484.1:p.Ala985=
XM_005266428.1:c.2936C=	XP_005266485.1:p.Ala979=
XM_005266430.3:c.3188C=	XP_005266487.1:p.Ala1063=
XM_005266431.2:c.3152C=	XP_005266488.1:p.Ala1051=
XM_005266432.2:c.2702C=	XP_005266489.1:p.Ala901=
XM_006719837.2:c.3092C=	XP_006719900.1:p.Ala1031=
XM_006719838.1:c.1004C=	XP_006719901.1:p.Ala335=
XM_006719839.1:c.877-1610C=	XP_006719902.1:n.877-1610C=
XM_011535117.1:c.3092C=	XP_011533419.1:p.Ala1031=
XM_011535118.1:c.3053C=	XP_011533420.1:p.Ala1018=
XM_011535119.1:c.3061-1610C=	XP_011533421.1:n.3061-1610C=
XM_011535120.1:c.2774C=	XP_011533422.1:p.Ala925=
XM_011535121.1:c.2731-1610C=	XP_011533423.1:n.2731-1610C=
XM_011535122.1:c.1856C=	XP_011533424.1:p.Ala619=
XR_941601.1:n.3407C=
XR_941602.1:n.3407C=
XR_941603.1:n.3407C=
XR_941604.1:n.3407C=
NM_001330578.1:c.2954C=	NP_001317507.1:p.Ala985=
NM_001330579.1:c.2936C=	NP_001317508.1:p.Ala979=
XM_005266424.4:c.3092C=	XP_005266481.1:p.Ala1031=
XM_005266430.4:c.3188C=	XP_005266487.1:p.Ala1063=
XM_005266431.4:c.3152C=	XP_005266488.1:p.Ala1051=
XM_006719837.3:c.3092C=	XP_006719900.1:p.Ala1031=
XM_011535117.3:c.3092C=	XP_011533419.1:p.Ala1031=
XM_017020627.1:c.3092C=	XP_016876116.1:p.Ala1031=
NM_000053.4:c.3188C= MANE Select	NP_000044.2:p.Ala1063=
NM_001005918.3:c.2567C=	NP_001005918.1:p.Ala856=
NM_001330579.2:c.2936C=	NP_001317508.1:p.Ala979=
NM_001243182.2:c.2855C=	NP_001230111.1:p.Ala952=
NM_001330578.2:c.2954C=	NP_001317507.1:p.Ala985=