Canonical Allele Identifier: CA483894660

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518293G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944157G>T , CM000675.2:g.51944157G>T	GRCh38
NC_000013.10:g.52518293G>T , CM000675.1:g.52518293G>T	GRCh37
NC_000013.9:g.51416294G>T	NCBI36
NG_008806.1:g.72338C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*894-1603C>A	ENSP00000489512.2:n.*894-1603C>A
ENST00000673864.2:c.*1939C>A	ENSP00000501045.2:n.*1939C>A
ENST00000674147.2:c.2574C>A	ENSP00000500964.2:p.Ala858=
ENST00000242839.10:c.3195C>A MANE Select	ENSP00000242839.5:p.Ala1065=
ENST00000344297.9:c.2574C>A	ENSP00000342559.5:p.Ala858=
ENST00000400366.6:c.2862C>A	ENSP00000383217.3:p.Ala954=
ENST00000448424.7:c.2943C>A	ENSP00000416738.3:p.Ala981=
ENST00000673772.1:c.2961C>A	ENSP00000501168.1:p.Ala987=
ENST00000673867.1:n.3334C>A
ENST00000674126.1:n.3558C>A
ENST00000674147.1:c.2130C>A	ENSP00000500964.1:p.Ala710=
ENST00000242839.8:c.3195C>A	ENSP00000242839.4:p.Ala1065=
ENST00000344297.8:c.2574C>A	ENSP00000342559.5:p.Ala858=
ENST00000400366.5:c.2862C>A	ENSP00000383217.3:p.Ala954=
ENST00000400370.8:c.1905C>A	ENSP00000383221.3:p.Ala635=
ENST00000418097.7:c.3000C>A	ENSP00000393343.2:p.Ala1000=
ENST00000448424.6:c.2961C>A	ENSP00000416738.2:p.Ala987=
ENST00000466629.1:n.415C>A
ENST00000634296.1:c.1022-1603C>A
ENST00000634308.1:c.*296C>A	ENSP00000489234.1:n.*296C>A
ENST00000634620.1:n.3939C>A
ENST00000634810.1:n.2540C>A
ENST00000634844.1:c.3051C>A	ENSP00000489398.1:p.Ala1017=
NM_000053.3:c.3195C>A	NP_000044.2:p.Ala1065=
NM_001005918.2:c.2574C>A	NP_001005918.1:p.Ala858=
NM_001243182.1:c.2862C>A	NP_001230111.1:p.Ala954=
XM_005266423.2:c.3099C>A	XP_005266480.1:p.Ala1033=
XM_005266424.3:c.3099C>A	XP_005266481.1:p.Ala1033=
XM_005266427.2:c.2961C>A	XP_005266484.1:p.Ala987=
XM_005266428.1:c.2943C>A	XP_005266485.1:p.Ala981=
XM_005266430.3:c.3195C>A	XP_005266487.1:p.Ala1065=
XM_005266431.2:c.3159C>A	XP_005266488.1:p.Ala1053=
XM_005266432.2:c.2709C>A	XP_005266489.1:p.Ala903=
XM_006719837.2:c.3099C>A	XP_006719900.1:p.Ala1033=
XM_006719838.1:c.1011C>A	XP_006719901.1:p.Ala337=
XM_006719839.1:c.877-1603C>A	XP_006719902.1:n.877-1603C>A
XM_011535117.1:c.3099C>A	XP_011533419.1:p.Ala1033=
XM_011535118.1:c.3060C>A	XP_011533420.1:p.Ala1020=
XM_011535119.1:c.3061-1603C>A	XP_011533421.1:n.3061-1603C>A
XM_011535120.1:c.2781C>A	XP_011533422.1:p.Ala927=
XM_011535121.1:c.2731-1603C>A	XP_011533423.1:n.2731-1603C>A
XM_011535122.1:c.1863C>A	XP_011533424.1:p.Ala621=
XR_941601.1:n.3414C>A
XR_941602.1:n.3414C>A
XR_941603.1:n.3414C>A
XR_941604.1:n.3414C>A
NM_001330578.1:c.2961C>A	NP_001317507.1:p.Ala987=
NM_001330579.1:c.2943C>A	NP_001317508.1:p.Ala981=
XM_005266424.4:c.3099C>A	XP_005266481.1:p.Ala1033=
XM_005266430.4:c.3195C>A	XP_005266487.1:p.Ala1065=
XM_005266431.4:c.3159C>A	XP_005266488.1:p.Ala1053=
XM_006719837.3:c.3099C>A	XP_006719900.1:p.Ala1033=
XM_011535117.3:c.3099C>A	XP_011533419.1:p.Ala1033=
XM_017020627.1:c.3099C>A	XP_016876116.1:p.Ala1033=
NM_000053.4:c.3195C>A MANE Select	NP_000044.2:p.Ala1065=
NM_001005918.3:c.2574C>A	NP_001005918.1:p.Ala858=
NM_001330579.2:c.2943C>A	NP_001317508.1:p.Ala981=
NM_001243182.2:c.2862C>A	NP_001230111.1:p.Ala954=
NM_001330578.2:c.2961C>A	NP_001317507.1:p.Ala987=