Canonical Allele Identifier: CA2091552997

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51970693T= , CM000675.2:g.51970693T=	GRCh38
NC_000013.10:g.52544829T= , CM000675.1:g.52544829T=	GRCh37
NC_000013.9:g.51442830T=	NCBI36
NG_008806.1:g.45802A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.1342A=	ENSP00000489512.2:p.Thr448=
ENST00000673864.2:c.*86A=	ENSP00000501045.2:n.*86A=
ENST00000674147.2:c.1342A=	ENSP00000500964.2:p.Thr448=
ENST00000242839.10:c.1342A= MANE Select	ENSP00000242839.5:p.Thr448=
ENST00000344297.9:c.1342A=	ENSP00000342559.5:p.Thr448=
ENST00000400366.6:c.1009A=	ENSP00000383217.3:p.Thr337=
ENST00000448424.7:c.1342A=	ENSP00000416738.3:p.Thr448=
ENST00000483772.2:n.98A=
ENST00000673772.1:c.1342A=	ENSP00000501168.1:p.Thr448=
ENST00000673789.1:n.298A=
ENST00000673864.1:c.536A=	ENSP00000501045.1:n.536A=
ENST00000674078.1:n.1443A=
ENST00000674147.1:c.898A=	ENSP00000500964.1:p.Thr300=
ENST00000242839.8:c.1342A=	ENSP00000242839.4:p.Thr448=
ENST00000344297.8:c.1342A=	ENSP00000342559.5:p.Thr448=
ENST00000400366.5:c.1009A=	ENSP00000383217.3:p.Thr337=
ENST00000400370.8:c.1285+3242A=	ENSP00000383221.3:n.1285+3242A=
ENST00000418097.7:c.1342A=	ENSP00000393343.2:p.Thr448=
ENST00000448424.6:c.1342A=	ENSP00000416738.2:p.Thr448=
ENST00000482841.6:n.1463A=
ENST00000483772.1:n.98A=
ENST00000634308.1:c.1342A=	ENSP00000489234.1:p.Thr448=
ENST00000634844.1:c.1342A=	ENSP00000489398.1:p.Thr448=
ENST00000635406.1:n.212-24215A=
NM_000053.3:c.1342A=	NP_000044.2:p.Thr448=
NM_001005918.2:c.1342A=	NP_001005918.1:p.Thr448=
NM_001243182.1:c.1009A=	NP_001230111.1:p.Thr337=
XM_005266423.2:c.1246A=	XP_005266480.1:p.Thr416=
XM_005266424.3:c.1246A=	XP_005266481.1:p.Thr416=
XM_005266427.2:c.1342A=	XP_005266484.1:p.Thr448=
XM_005266428.1:c.1342A=	XP_005266485.1:p.Thr448=
XM_005266430.3:c.1342A=	XP_005266487.1:p.Thr448=
XM_005266431.2:c.1306A=	XP_005266488.1:p.Thr436=
XM_005266432.2:c.1342A=	XP_005266489.1:p.Thr448=
XM_006719837.2:c.1246A=	XP_006719900.1:p.Thr416=
XM_011535117.1:c.1246A=	XP_011533419.1:p.Thr416=
XM_011535118.1:c.1342A=	XP_011533420.1:p.Thr448=
XM_011535119.1:c.1342A=	XP_011533421.1:p.Thr448=
XM_011535120.1:c.1342A=	XP_011533422.1:p.Thr448=
XM_011535121.1:c.1342A=	XP_011533423.1:p.Thr448=
XM_011535122.1:c.10A=	XP_011533424.1:p.Thr4=
XR_941601.1:n.1561A=
XR_941602.1:n.1561A=
XR_941603.1:n.1561A=
XR_941604.1:n.1561A=
NM_001330578.1:c.1342A=	NP_001317507.1:p.Thr448=
NM_001330579.1:c.1342A=	NP_001317508.1:p.Thr448=
XM_005266424.4:c.1246A=	XP_005266481.1:p.Thr416=
XM_005266430.4:c.1342A=	XP_005266487.1:p.Thr448=
XM_005266431.4:c.1306A=	XP_005266488.1:p.Thr436=
XM_006719837.3:c.1246A=	XP_006719900.1:p.Thr416=
XM_011535117.3:c.1246A=	XP_011533419.1:p.Thr416=
XM_017020627.1:c.1246A=	XP_016876116.1:p.Thr416=
NM_000053.4:c.1342A= MANE Select	NP_000044.2:p.Thr448=
NM_001005918.3:c.1342A=	NP_001005918.1:p.Thr448=
NM_001330579.2:c.1342A=	NP_001317508.1:p.Thr448=
NM_001243182.2:c.1009A=	NP_001230111.1:p.Thr337=
NM_001330578.2:c.1342A=	NP_001317507.1:p.Thr448=