Canonical Allele Identifier: CA2091563886

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944174C= , CM000675.2:g.51944174C=	GRCh38
NC_000013.10:g.52518310C= , CM000675.1:g.52518310C=	GRCh37
NC_000013.9:g.51416311C=	NCBI36
NG_008806.1:g.72321G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1620G=	ENSP00000489512.2:n.*894-1620G=
ENST00000673864.2:c.*1922G=	ENSP00000501045.2:n.*1922G=
ENST00000674147.2:c.2557G=	ENSP00000500964.2:p.Val853=
ENST00000242839.10:c.3178G= MANE Select	ENSP00000242839.5:p.Val1060=
ENST00000344297.9:c.2557G=	ENSP00000342559.5:p.Val853=
ENST00000400366.6:c.2845G=	ENSP00000383217.3:p.Val949=
ENST00000448424.7:c.2926G=	ENSP00000416738.3:p.Val976=
ENST00000673772.1:c.2944G=	ENSP00000501168.1:p.Val982=
ENST00000673867.1:n.3317G=
ENST00000674126.1:n.3541G=
ENST00000674147.1:c.2113G=	ENSP00000500964.1:p.Val705=
ENST00000242839.8:c.3178G=	ENSP00000242839.4:p.Val1060=
ENST00000344297.8:c.2557G=	ENSP00000342559.5:p.Val853=
ENST00000400366.5:c.2845G=	ENSP00000383217.3:p.Val949=
ENST00000400370.8:c.1888G=	ENSP00000383221.3:p.Val630=
ENST00000418097.7:c.2983G=	ENSP00000393343.2:p.Val995=
ENST00000448424.6:c.2944G=	ENSP00000416738.2:p.Val982=
ENST00000466629.1:n.398G=
ENST00000634296.1:c.1022-1620G=
ENST00000634308.1:c.*279G=	ENSP00000489234.1:n.*279G=
ENST00000634620.1:n.3922G=
ENST00000634810.1:n.2523G=
ENST00000634844.1:c.3034G=	ENSP00000489398.1:p.Val1012=
NM_000053.3:c.3178G=	NP_000044.2:p.Val1060=
NM_001005918.2:c.2557G=	NP_001005918.1:p.Val853=
NM_001243182.1:c.2845G=	NP_001230111.1:p.Val949=
XM_005266423.2:c.3082G=	XP_005266480.1:p.Val1028=
XM_005266424.3:c.3082G=	XP_005266481.1:p.Val1028=
XM_005266427.2:c.2944G=	XP_005266484.1:p.Val982=
XM_005266428.1:c.2926G=	XP_005266485.1:p.Val976=
XM_005266430.3:c.3178G=	XP_005266487.1:p.Val1060=
XM_005266431.2:c.3142G=	XP_005266488.1:p.Val1048=
XM_005266432.2:c.2692G=	XP_005266489.1:p.Val898=
XM_006719837.2:c.3082G=	XP_006719900.1:p.Val1028=
XM_006719838.1:c.994G=	XP_006719901.1:p.Val332=
XM_006719839.1:c.877-1620G=	XP_006719902.1:n.877-1620G=
XM_011535117.1:c.3082G=	XP_011533419.1:p.Val1028=
XM_011535118.1:c.3043G=	XP_011533420.1:p.Val1015=
XM_011535119.1:c.3061-1620G=	XP_011533421.1:n.3061-1620G=
XM_011535120.1:c.2764G=	XP_011533422.1:p.Val922=
XM_011535121.1:c.2731-1620G=	XP_011533423.1:n.2731-1620G=
XM_011535122.1:c.1846G=	XP_011533424.1:p.Val616=
XR_941601.1:n.3397G=
XR_941602.1:n.3397G=
XR_941603.1:n.3397G=
XR_941604.1:n.3397G=
NM_001330578.1:c.2944G=	NP_001317507.1:p.Val982=
NM_001330579.1:c.2926G=	NP_001317508.1:p.Val976=
XM_005266424.4:c.3082G=	XP_005266481.1:p.Val1028=
XM_005266430.4:c.3178G=	XP_005266487.1:p.Val1060=
XM_005266431.4:c.3142G=	XP_005266488.1:p.Val1048=
XM_006719837.3:c.3082G=	XP_006719900.1:p.Val1028=
XM_011535117.3:c.3082G=	XP_011533419.1:p.Val1028=
XM_017020627.1:c.3082G=	XP_016876116.1:p.Val1028=
NM_000053.4:c.3178G= MANE Select	NP_000044.2:p.Val1060=
NM_001005918.3:c.2557G=	NP_001005918.1:p.Val853=
NM_001330579.2:c.2926G=	NP_001317508.1:p.Val976=
NM_001243182.2:c.2845G=	NP_001230111.1:p.Val949=
NM_001330578.2:c.2944G=	NP_001317507.1:p.Val982=