Canonical Allele Identifier: CA388023878

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513231T>A (hg19) ; chr13:g.51939095T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939095T>A , CM000675.2:g.51939095T>A	GRCh38
NC_000013.10:g.52513231T>A , CM000675.1:g.52513231T>A	GRCh37
NC_000013.9:g.51411232T>A	NCBI36
NG_008806.1:g.77400A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1305A>T	ENSP00000489512.2:n.*1305A>T
ENST00000673864.2:c.*2399A>T	ENSP00000501045.2:n.*2399A>T
ENST00000674147.2:c.3034A>T	ENSP00000500964.2:p.Ile1012Phe
ENST00000242839.10:c.3655A>T MANE Select	ENSP00000242839.5:p.Ile1219Phe
ENST00000344297.9:c.3034A>T	ENSP00000342559.5:p.Ile1012Phe
ENST00000400366.6:c.3322A>T	ENSP00000383217.3:p.Ile1108Phe
ENST00000448424.7:c.3403A>T	ENSP00000416738.3:p.Ile1135Phe
ENST00000673696.1:n.896A>T
ENST00000673772.1:c.3421A>T	ENSP00000501168.1:p.Ile1141Phe
ENST00000673867.1:n.3794A>T
ENST00000673923.1:n.521A>T
ENST00000674147.1:c.2590A>T	ENSP00000500964.1:p.Ile864Phe
ENST00000242839.8:c.3655A>T	ENSP00000242839.4:p.Ile1219Phe
ENST00000344297.8:c.3034A>T	ENSP00000342559.5:p.Ile1012Phe
ENST00000400366.5:c.3322A>T	ENSP00000383217.3:p.Ile1108Phe
ENST00000400370.8:c.2365A>T	ENSP00000383221.3:p.Ile789Phe
ENST00000418097.7:c.3460A>T	ENSP00000393343.2:p.Ile1154Phe
ENST00000448424.6:c.3421A>T	ENSP00000416738.2:p.Ile1141Phe
ENST00000634296.1:c.1433A>T
ENST00000634308.1:c.*756A>T	ENSP00000489234.1:n.*756A>T
ENST00000634620.1:n.4399A>T
ENST00000634810.1:n.3000A>T
ENST00000634844.1:c.3511A>T	ENSP00000489398.1:p.Ile1171Phe
NM_000053.3:c.3655A>T	NP_000044.2:p.Ile1219Phe
NM_001005918.2:c.3034A>T	NP_001005918.1:p.Ile1012Phe
NM_001243182.1:c.3322A>T	NP_001230111.1:p.Ile1108Phe
XM_005266423.2:c.3559A>T	XP_005266480.1:p.Ile1187Phe
XM_005266424.3:c.3559A>T	XP_005266481.1:p.Ile1187Phe
XM_005266427.2:c.3421A>T	XP_005266484.1:p.Ile1141Phe
XM_005266428.1:c.3403A>T	XP_005266485.1:p.Ile1135Phe
XM_005266430.3:c.3655A>T	XP_005266487.1:p.Ile1219Phe
XM_005266431.2:c.3619A>T	XP_005266488.1:p.Ile1207Phe
XM_005266432.2:c.3169A>T	XP_005266489.1:p.Ile1057Phe
XM_006719837.2:c.3559A>T	XP_006719900.1:p.Ile1187Phe
XM_006719838.1:c.1471A>T	XP_006719901.1:p.Ile491Phe
XM_006719839.1:c.1288A>T	XP_006719902.1:p.Ile430Phe
XM_011535117.1:c.3559A>T	XP_011533419.1:p.Ile1187Phe
XM_011535118.1:c.3520A>T	XP_011533420.1:p.Ile1174Phe
XM_011535119.1:c.3472A>T	XP_011533421.1:p.Ile1158Phe
XM_011535120.1:c.3241A>T	XP_011533422.1:p.Ile1081Phe
XM_011535121.1:c.3142A>T	XP_011533423.1:p.Ile1048Phe
XM_011535122.1:c.2323A>T	XP_011533424.1:p.Ile775Phe
XR_941601.1:n.3874A>T
XR_941602.1:n.3874A>T
XR_941603.1:n.3874A>T
XR_941604.1:n.3874A>T
NM_001330578.1:c.3421A>T	NP_001317507.1:p.Ile1141Phe
NM_001330579.1:c.3403A>T	NP_001317508.1:p.Ile1135Phe
XM_005266424.4:c.3559A>T	XP_005266481.1:p.Ile1187Phe
XM_005266430.4:c.3655A>T	XP_005266487.1:p.Ile1219Phe
XM_005266431.4:c.3619A>T	XP_005266488.1:p.Ile1207Phe
XM_006719837.3:c.3559A>T	XP_006719900.1:p.Ile1187Phe
XM_011535117.3:c.3559A>T	XP_011533419.1:p.Ile1187Phe
XM_017020627.1:c.3559A>T	XP_016876116.1:p.Ile1187Phe
NM_000053.4:c.3655A>T MANE Select	NP_000044.2:p.Ile1219Phe
NM_001005918.3:c.3034A>T	NP_001005918.1:p.Ile1012Phe
NM_001330579.2:c.3403A>T	NP_001317508.1:p.Ile1135Phe
NM_001243182.2:c.3322A>T	NP_001230111.1:p.Ile1108Phe
NM_001330578.2:c.3421A>T	NP_001317507.1:p.Ile1141Phe