Canonical Allele Identifier: CA2091564253

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944281A= , CM000675.2:g.51944281A=	GRCh38
NC_000013.10:g.52518417A= , CM000675.1:g.52518417A=	GRCh37
NC_000013.9:g.51416418A=	NCBI36
NG_008806.1:g.72214T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1727T=	ENSP00000489512.2:n.*894-1727T=
ENST00000673864.2:c.*1815T=	ENSP00000501045.2:n.*1815T=
ENST00000674147.2:c.2450T=	ENSP00000500964.2:p.Val817=
ENST00000242839.10:c.3071T= MANE Select	ENSP00000242839.5:p.Val1024=
ENST00000344297.9:c.2450T=	ENSP00000342559.5:p.Val817=
ENST00000400366.6:c.2738T=	ENSP00000383217.3:p.Val913=
ENST00000448424.7:c.2819T=	ENSP00000416738.3:p.Val940=
ENST00000673772.1:c.2837T=	ENSP00000501168.1:p.Val946=
ENST00000673867.1:n.3210T=
ENST00000674126.1:n.3434T=
ENST00000674147.1:c.2006T=	ENSP00000500964.1:p.Val669=
ENST00000242839.8:c.3071T=	ENSP00000242839.4:p.Val1024=
ENST00000344297.8:c.2450T=	ENSP00000342559.5:p.Val817=
ENST00000400366.5:c.2738T=	ENSP00000383217.3:p.Val913=
ENST00000400370.8:c.1781T=	ENSP00000383221.3:p.Val594=
ENST00000418097.7:c.2876T=	ENSP00000393343.2:p.Val959=
ENST00000448424.6:c.2837T=	ENSP00000416738.2:p.Val946=
ENST00000466629.1:n.291T=
ENST00000634296.1:c.1022-1727T=
ENST00000634308.1:c.*172T=	ENSP00000489234.1:n.*172T=
ENST00000634620.1:n.3815T=
ENST00000634810.1:n.2416T=
ENST00000634844.1:c.2927T=	ENSP00000489398.1:p.Val976=
ENST00000635406.1:n.417T=
NM_000053.3:c.3071T=	NP_000044.2:p.Val1024=
NM_001005918.2:c.2450T=	NP_001005918.1:p.Val817=
NM_001243182.1:c.2738T=	NP_001230111.1:p.Val913=
XM_005266423.2:c.2975T=	XP_005266480.1:p.Val992=
XM_005266424.3:c.2975T=	XP_005266481.1:p.Val992=
XM_005266427.2:c.2837T=	XP_005266484.1:p.Val946=
XM_005266428.1:c.2819T=	XP_005266485.1:p.Val940=
XM_005266430.3:c.3071T=	XP_005266487.1:p.Val1024=
XM_005266431.2:c.3035T=	XP_005266488.1:p.Val1012=
XM_005266432.2:c.2585T=	XP_005266489.1:p.Val862=
XM_006719837.2:c.2975T=	XP_006719900.1:p.Val992=
XM_006719838.1:c.887T=	XP_006719901.1:p.Val296=
XM_006719839.1:c.877-1727T=	XP_006719902.1:n.877-1727T=
XM_011535117.1:c.2975T=	XP_011533419.1:p.Val992=
XM_011535118.1:c.2936T=	XP_011533420.1:p.Val979=
XM_011535119.1:c.3061-1727T=	XP_011533421.1:n.3061-1727T=
XM_011535120.1:c.2657T=	XP_011533422.1:p.Val886=
XM_011535121.1:c.2731-1727T=	XP_011533423.1:n.2731-1727T=
XM_011535122.1:c.1739T=	XP_011533424.1:p.Val580=
XR_941601.1:n.3290T=
XR_941602.1:n.3290T=
XR_941603.1:n.3290T=
XR_941604.1:n.3290T=
NM_001330578.1:c.2837T=	NP_001317507.1:p.Val946=
NM_001330579.1:c.2819T=	NP_001317508.1:p.Val940=
XM_005266424.4:c.2975T=	XP_005266481.1:p.Val992=
XM_005266430.4:c.3071T=	XP_005266487.1:p.Val1024=
XM_005266431.4:c.3035T=	XP_005266488.1:p.Val1012=
XM_006719837.3:c.2975T=	XP_006719900.1:p.Val992=
XM_011535117.3:c.2975T=	XP_011533419.1:p.Val992=
XM_017020627.1:c.2975T=	XP_016876116.1:p.Val992=
NM_000053.4:c.3071T= MANE Select	NP_000044.2:p.Val1024=
NM_001005918.3:c.2450T=	NP_001005918.1:p.Val817=
NM_001330579.2:c.2819T=	NP_001317508.1:p.Val940=
NM_001243182.2:c.2738T=	NP_001230111.1:p.Val913=
NM_001330578.2:c.2837T=	NP_001317507.1:p.Val946=