Canonical Allele Identifier: CA2091559357

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941104G= , CM000675.2:g.51941104G=	GRCh38
NC_000013.10:g.52515240G= , CM000675.1:g.52515240G=	GRCh37
NC_000013.9:g.51413241G=	NCBI36
NG_008806.1:g.75391C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1183C=	ENSP00000489512.2:n.*1183C=
ENST00000673864.2:c.*2277C=	ENSP00000501045.2:n.*2277C=
ENST00000674147.2:c.2912C=	ENSP00000500964.2:p.Thr971=
ENST00000242839.10:c.3533C= MANE Select	ENSP00000242839.5:p.Thr1178=
ENST00000344297.9:c.2912C=	ENSP00000342559.5:p.Thr971=
ENST00000400366.6:c.3200C=	ENSP00000383217.3:p.Thr1067=
ENST00000448424.7:c.3281C=	ENSP00000416738.3:p.Thr1094=
ENST00000673772.1:c.3299C=	ENSP00000501168.1:p.Thr1100=
ENST00000673867.1:n.3672C=
ENST00000674126.1:n.3896C=
ENST00000674147.1:c.2468C=	ENSP00000500964.1:p.Thr823=
ENST00000242839.8:c.3533C=	ENSP00000242839.4:p.Thr1178=
ENST00000344297.8:c.2912C=	ENSP00000342559.5:p.Thr971=
ENST00000400366.5:c.3200C=	ENSP00000383217.3:p.Thr1067=
ENST00000400370.8:c.2243C=	ENSP00000383221.3:p.Thr748=
ENST00000418097.7:c.3338C=	ENSP00000393343.2:p.Thr1113=
ENST00000448424.6:c.3299C=	ENSP00000416738.2:p.Thr1100=
ENST00000634296.1:c.1311C=
ENST00000634308.1:c.*634C=	ENSP00000489234.1:n.*634C=
ENST00000634620.1:n.4277C=
ENST00000634810.1:n.2878C=
ENST00000634844.1:c.3389C=	ENSP00000489398.1:p.Thr1130=
NM_000053.3:c.3533C=	NP_000044.2:p.Thr1178=
NM_001005918.2:c.2912C=	NP_001005918.1:p.Thr971=
NM_001243182.1:c.3200C=	NP_001230111.1:p.Thr1067=
XM_005266423.2:c.3437C=	XP_005266480.1:p.Thr1146=
XM_005266424.3:c.3437C=	XP_005266481.1:p.Thr1146=
XM_005266427.2:c.3299C=	XP_005266484.1:p.Thr1100=
XM_005266428.1:c.3281C=	XP_005266485.1:p.Thr1094=
XM_005266430.3:c.3533C=	XP_005266487.1:p.Thr1178=
XM_005266431.2:c.3497C=	XP_005266488.1:p.Thr1166=
XM_005266432.2:c.3047C=	XP_005266489.1:p.Thr1016=
XM_006719837.2:c.3437C=	XP_006719900.1:p.Thr1146=
XM_006719838.1:c.1349C=	XP_006719901.1:p.Thr450=
XM_006719839.1:c.1166C=	XP_006719902.1:p.Thr389=
XM_011535117.1:c.3437C=	XP_011533419.1:p.Thr1146=
XM_011535118.1:c.3398C=	XP_011533420.1:p.Thr1133=
XM_011535119.1:c.3350C=	XP_011533421.1:p.Thr1117=
XM_011535120.1:c.3119C=	XP_011533422.1:p.Thr1040=
XM_011535121.1:c.3020C=	XP_011533423.1:p.Thr1007=
XM_011535122.1:c.2201C=	XP_011533424.1:p.Thr734=
XR_941601.1:n.3752C=
XR_941602.1:n.3752C=
XR_941603.1:n.3752C=
XR_941604.1:n.3752C=
NM_001330578.1:c.3299C=	NP_001317507.1:p.Thr1100=
NM_001330579.1:c.3281C=	NP_001317508.1:p.Thr1094=
XM_005266424.4:c.3437C=	XP_005266481.1:p.Thr1146=
XM_005266430.4:c.3533C=	XP_005266487.1:p.Thr1178=
XM_005266431.4:c.3497C=	XP_005266488.1:p.Thr1166=
XM_006719837.3:c.3437C=	XP_006719900.1:p.Thr1146=
XM_011535117.3:c.3437C=	XP_011533419.1:p.Thr1146=
XM_017020627.1:c.3437C=	XP_016876116.1:p.Thr1146=
NM_000053.4:c.3533C= MANE Select	NP_000044.2:p.Thr1178=
NM_001005918.3:c.2912C=	NP_001005918.1:p.Thr971=
NM_001330579.2:c.3281C=	NP_001317508.1:p.Thr1094=
NM_001243182.2:c.3200C=	NP_001230111.1:p.Thr1067=
NM_001330578.2:c.3299C=	NP_001317507.1:p.Thr1100=