Canonical Allele Identifier: CA2091559518

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941174T= , CM000675.2:g.51941174T=	GRCh38
NC_000013.10:g.52515310T= , CM000675.1:g.52515310T=	GRCh37
NC_000013.9:g.51413311T=	NCBI36
NG_008806.1:g.75321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1113A=	ENSP00000489512.2:n.*1113A=
ENST00000673864.2:c.*2207A=	ENSP00000501045.2:n.*2207A=
ENST00000674147.2:c.2842A=	ENSP00000500964.2:p.Arg948=
ENST00000242839.10:c.3463A= MANE Select	ENSP00000242839.5:p.Arg1155=
ENST00000344297.9:c.2842A=	ENSP00000342559.5:p.Arg948=
ENST00000400366.6:c.3130A=	ENSP00000383217.3:p.Arg1044=
ENST00000448424.7:c.3211A=	ENSP00000416738.3:p.Arg1071=
ENST00000673772.1:c.3229A=	ENSP00000501168.1:p.Arg1077=
ENST00000673867.1:n.3602A=
ENST00000674126.1:n.3826A=
ENST00000674147.1:c.2398A=	ENSP00000500964.1:p.Arg800=
ENST00000242839.8:c.3463A=	ENSP00000242839.4:p.Arg1155=
ENST00000344297.8:c.2842A=	ENSP00000342559.5:p.Arg948=
ENST00000400366.5:c.3130A=	ENSP00000383217.3:p.Arg1044=
ENST00000400370.8:c.2173A=	ENSP00000383221.3:p.Arg725=
ENST00000418097.7:c.3268A=	ENSP00000393343.2:p.Arg1090=
ENST00000448424.6:c.3229A=	ENSP00000416738.2:p.Arg1077=
ENST00000634296.1:c.1241A=
ENST00000634308.1:c.*564A=	ENSP00000489234.1:n.*564A=
ENST00000634620.1:n.4207A=
ENST00000634810.1:n.2808A=
ENST00000634844.1:c.3319A=	ENSP00000489398.1:p.Arg1107=
NM_000053.3:c.3463A=	NP_000044.2:p.Arg1155=
NM_001005918.2:c.2842A=	NP_001005918.1:p.Arg948=
NM_001243182.1:c.3130A=	NP_001230111.1:p.Arg1044=
XM_005266423.2:c.3367A=	XP_005266480.1:p.Arg1123=
XM_005266424.3:c.3367A=	XP_005266481.1:p.Arg1123=
XM_005266427.2:c.3229A=	XP_005266484.1:p.Arg1077=
XM_005266428.1:c.3211A=	XP_005266485.1:p.Arg1071=
XM_005266430.3:c.3463A=	XP_005266487.1:p.Arg1155=
XM_005266431.2:c.3427A=	XP_005266488.1:p.Arg1143=
XM_005266432.2:c.2977A=	XP_005266489.1:p.Arg993=
XM_006719837.2:c.3367A=	XP_006719900.1:p.Arg1123=
XM_006719838.1:c.1279A=	XP_006719901.1:p.Arg427=
XM_006719839.1:c.1096A=	XP_006719902.1:p.Arg366=
XM_011535117.1:c.3367A=	XP_011533419.1:p.Arg1123=
XM_011535118.1:c.3328A=	XP_011533420.1:p.Arg1110=
XM_011535119.1:c.3280A=	XP_011533421.1:p.Arg1094=
XM_011535120.1:c.3049A=	XP_011533422.1:p.Arg1017=
XM_011535121.1:c.2950A=	XP_011533423.1:p.Arg984=
XM_011535122.1:c.2131A=	XP_011533424.1:p.Arg711=
XR_941601.1:n.3682A=
XR_941602.1:n.3682A=
XR_941603.1:n.3682A=
XR_941604.1:n.3682A=
NM_001330578.1:c.3229A=	NP_001317507.1:p.Arg1077=
NM_001330579.1:c.3211A=	NP_001317508.1:p.Arg1071=
XM_005266424.4:c.3367A=	XP_005266481.1:p.Arg1123=
XM_005266430.4:c.3463A=	XP_005266487.1:p.Arg1155=
XM_005266431.4:c.3427A=	XP_005266488.1:p.Arg1143=
XM_006719837.3:c.3367A=	XP_006719900.1:p.Arg1123=
XM_011535117.3:c.3367A=	XP_011533419.1:p.Arg1123=
XM_017020627.1:c.3367A=	XP_016876116.1:p.Arg1123=
NM_000053.4:c.3463A= MANE Select	NP_000044.2:p.Arg1155=
NM_001005918.3:c.2842A=	NP_001005918.1:p.Arg948=
NM_001330579.2:c.3211A=	NP_001317508.1:p.Arg1071=
NM_001243182.2:c.3130A=	NP_001230111.1:p.Arg1044=
NM_001330578.2:c.3229A=	NP_001317507.1:p.Arg1077=