Canonical Allele Identifier: CA483894755

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518395G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944259G>A , CM000675.2:g.51944259G>A	GRCh38
NC_000013.10:g.52518395G>A , CM000675.1:g.52518395G>A	GRCh37
NC_000013.9:g.51416396G>A	NCBI36
NG_008806.1:g.72236C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1705C>T	ENSP00000489512.2:n.*894-1705C>T
ENST00000673864.2:c.*1837C>T	ENSP00000501045.2:n.*1837C>T
ENST00000674147.2:c.2472C>T	ENSP00000500964.2:p.Thr824=
ENST00000242839.10:c.3093C>T MANE Select	ENSP00000242839.5:p.Thr1031=
ENST00000344297.9:c.2472C>T	ENSP00000342559.5:p.Thr824=
ENST00000400366.6:c.2760C>T	ENSP00000383217.3:p.Thr920=
ENST00000448424.7:c.2841C>T	ENSP00000416738.3:p.Thr947=
ENST00000673772.1:c.2859C>T	ENSP00000501168.1:p.Thr953=
ENST00000673867.1:n.3232C>T
ENST00000674126.1:n.3456C>T
ENST00000674147.1:c.2028C>T	ENSP00000500964.1:p.Thr676=
ENST00000242839.8:c.3093C>T	ENSP00000242839.4:p.Thr1031=
ENST00000344297.8:c.2472C>T	ENSP00000342559.5:p.Thr824=
ENST00000400366.5:c.2760C>T	ENSP00000383217.3:p.Thr920=
ENST00000400370.8:c.1803C>T	ENSP00000383221.3:p.Thr601=
ENST00000418097.7:c.2898C>T	ENSP00000393343.2:p.Thr966=
ENST00000448424.6:c.2859C>T	ENSP00000416738.2:p.Thr953=
ENST00000466629.1:n.313C>T
ENST00000634296.1:c.1022-1705C>T
ENST00000634308.1:c.*194C>T	ENSP00000489234.1:n.*194C>T
ENST00000634620.1:n.3837C>T
ENST00000634810.1:n.2438C>T
ENST00000634844.1:c.2949C>T	ENSP00000489398.1:p.Thr983=
ENST00000635406.1:n.439C>T
NM_000053.3:c.3093C>T	NP_000044.2:p.Thr1031=
NM_001005918.2:c.2472C>T	NP_001005918.1:p.Thr824=
NM_001243182.1:c.2760C>T	NP_001230111.1:p.Thr920=
XM_005266423.2:c.2997C>T	XP_005266480.1:p.Thr999=
XM_005266424.3:c.2997C>T	XP_005266481.1:p.Thr999=
XM_005266427.2:c.2859C>T	XP_005266484.1:p.Thr953=
XM_005266428.1:c.2841C>T	XP_005266485.1:p.Thr947=
XM_005266430.3:c.3093C>T	XP_005266487.1:p.Thr1031=
XM_005266431.2:c.3057C>T	XP_005266488.1:p.Thr1019=
XM_005266432.2:c.2607C>T	XP_005266489.1:p.Thr869=
XM_006719837.2:c.2997C>T	XP_006719900.1:p.Thr999=
XM_006719838.1:c.909C>T	XP_006719901.1:p.Thr303=
XM_006719839.1:c.877-1705C>T	XP_006719902.1:n.877-1705C>T
XM_011535117.1:c.2997C>T	XP_011533419.1:p.Thr999=
XM_011535118.1:c.2958C>T	XP_011533420.1:p.Thr986=
XM_011535119.1:c.3061-1705C>T	XP_011533421.1:n.3061-1705C>T
XM_011535120.1:c.2679C>T	XP_011533422.1:p.Thr893=
XM_011535121.1:c.2731-1705C>T	XP_011533423.1:n.2731-1705C>T
XM_011535122.1:c.1761C>T	XP_011533424.1:p.Thr587=
XR_941601.1:n.3312C>T
XR_941602.1:n.3312C>T
XR_941603.1:n.3312C>T
XR_941604.1:n.3312C>T
NM_001330578.1:c.2859C>T	NP_001317507.1:p.Thr953=
NM_001330579.1:c.2841C>T	NP_001317508.1:p.Thr947=
XM_005266424.4:c.2997C>T	XP_005266481.1:p.Thr999=
XM_005266430.4:c.3093C>T	XP_005266487.1:p.Thr1031=
XM_005266431.4:c.3057C>T	XP_005266488.1:p.Thr1019=
XM_006719837.3:c.2997C>T	XP_006719900.1:p.Thr999=
XM_011535117.3:c.2997C>T	XP_011533419.1:p.Thr999=
XM_017020627.1:c.2997C>T	XP_016876116.1:p.Thr999=
NM_000053.4:c.3093C>T MANE Select	NP_000044.2:p.Thr1031=
NM_001005918.3:c.2472C>T	NP_001005918.1:p.Thr824=
NM_001330579.2:c.2841C>T	NP_001317508.1:p.Thr947=
NM_001243182.2:c.2760C>T	NP_001230111.1:p.Thr920=
NM_001330578.2:c.2859C>T	NP_001317507.1:p.Thr953=