Canonical Allele Identifier: CA2091566199

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946415T= , CM000675.2:g.51946415T=	GRCh38
NC_000013.10:g.52520551T= , CM000675.1:g.52520551T=	GRCh37
NC_000013.9:g.51418552T=	NCBI36
NG_008806.1:g.70080A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*762A=	ENSP00000489512.2:n.*762A=
ENST00000673864.2:c.*1673A=	ENSP00000501045.2:n.*1673A=
ENST00000674147.2:c.2308A=	ENSP00000500964.2:p.Thr770=
ENST00000242839.10:c.2929A= MANE Select	ENSP00000242839.5:p.Thr977=
ENST00000344297.9:c.2308A=	ENSP00000342559.5:p.Thr770=
ENST00000400366.6:c.2596A=	ENSP00000383217.3:p.Thr866=
ENST00000448424.7:c.2677A=	ENSP00000416738.3:p.Thr893=
ENST00000673772.1:c.2695A=	ENSP00000501168.1:p.Thr899=
ENST00000673867.1:n.1076A=
ENST00000674126.1:n.3292A=
ENST00000674147.1:c.1864A=	ENSP00000500964.1:p.Thr622=
ENST00000242839.8:c.2929A=	ENSP00000242839.4:p.Thr977=
ENST00000344297.8:c.2308A=	ENSP00000342559.5:p.Thr770=
ENST00000400366.5:c.2596A=	ENSP00000383217.3:p.Thr866=
ENST00000400370.8:c.1639A=	ENSP00000383221.3:p.Thr547=
ENST00000418097.7:c.2866-2124A=	ENSP00000393343.2:n.2866-2124A=
ENST00000448424.6:c.2695A=	ENSP00000416738.2:p.Thr899=
ENST00000466629.1:n.149A=
ENST00000634296.1:c.890A=
ENST00000634308.1:c.*30A=	ENSP00000489234.1:n.*30A=
ENST00000634620.1:n.3673A=
ENST00000634810.1:n.2274A=
ENST00000634844.1:c.2785A=	ENSP00000489398.1:p.Thr929=
ENST00000635406.1:n.275A=
NM_000053.3:c.2929A=	NP_000044.2:p.Thr977=
NM_001005918.2:c.2308A=	NP_001005918.1:p.Thr770=
NM_001243182.1:c.2596A=	NP_001230111.1:p.Thr866=
XM_005266423.2:c.2833A=	XP_005266480.1:p.Thr945=
XM_005266424.3:c.2833A=	XP_005266481.1:p.Thr945=
XM_005266427.2:c.2695A=	XP_005266484.1:p.Thr899=
XM_005266428.1:c.2677A=	XP_005266485.1:p.Thr893=
XM_005266430.3:c.2929A=	XP_005266487.1:p.Thr977=
XM_005266431.2:c.2893A=	XP_005266488.1:p.Thr965=
XM_005266432.2:c.2443A=	XP_005266489.1:p.Thr815=
XM_006719837.2:c.2833A=	XP_006719900.1:p.Thr945=
XM_006719838.1:c.745A=	XP_006719901.1:p.Thr249=
XM_006719839.1:c.745A=	XP_006719902.1:p.Thr249=
XM_011535117.1:c.2833A=	XP_011533419.1:p.Thr945=
XM_011535118.1:c.2794A=	XP_011533420.1:p.Thr932=
XM_011535119.1:c.2929A=	XP_011533421.1:p.Thr977=
XM_011535120.1:c.2515A=	XP_011533422.1:p.Thr839=
XM_011535121.1:c.2730+3592A=	XP_011533423.1:n.2730+3592A=
XM_011535122.1:c.1597A=	XP_011533424.1:p.Thr533=
XR_941601.1:n.3148A=
XR_941602.1:n.3148A=
XR_941603.1:n.3148A=
XR_941604.1:n.3148A=
NM_001330578.1:c.2695A=	NP_001317507.1:p.Thr899=
NM_001330579.1:c.2677A=	NP_001317508.1:p.Thr893=
XM_005266424.4:c.2833A=	XP_005266481.1:p.Thr945=
XM_005266430.4:c.2929A=	XP_005266487.1:p.Thr977=
XM_005266431.4:c.2893A=	XP_005266488.1:p.Thr965=
XM_006719837.3:c.2833A=	XP_006719900.1:p.Thr945=
XM_011535117.3:c.2833A=	XP_011533419.1:p.Thr945=
XM_017020627.1:c.2833A=	XP_016876116.1:p.Thr945=
NM_000053.4:c.2929A= MANE Select	NP_000044.2:p.Thr977=
NM_001005918.3:c.2308A=	NP_001005918.1:p.Thr770=
NM_001330579.2:c.2677A=	NP_001317508.1:p.Thr893=
NM_001243182.2:c.2596A=	NP_001230111.1:p.Thr866=
NM_001330578.2:c.2695A=	NP_001317507.1:p.Thr899=