Canonical Allele Identifier: CA388023869

Gene: ATP7B

Linked Data

• dbSNP Id: rs1957154912
• MyVariant Identifiers: chr13:g.52513230A>T (hg19) ; chr13:g.51939094A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939094A>T , CM000675.2:g.51939094A>T	GRCh38
NC_000013.10:g.52513230A>T , CM000675.1:g.52513230A>T	GRCh37
NC_000013.9:g.51411231A>T	NCBI36
NG_008806.1:g.77401T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1306T>A	ENSP00000489512.2:n.*1306T>A
ENST00000673864.2:c.*2400T>A	ENSP00000501045.2:n.*2400T>A
ENST00000674147.2:c.3035T>A	ENSP00000500964.2:p.Ile1012Asn
ENST00000242839.10:c.3656T>A MANE Select	ENSP00000242839.5:p.Ile1219Asn
ENST00000344297.9:c.3035T>A	ENSP00000342559.5:p.Ile1012Asn
ENST00000400366.6:c.3323T>A	ENSP00000383217.3:p.Ile1108Asn
ENST00000448424.7:c.3404T>A	ENSP00000416738.3:p.Ile1135Asn
ENST00000673696.1:n.897T>A
ENST00000673772.1:c.3422T>A	ENSP00000501168.1:p.Ile1141Asn
ENST00000673867.1:n.3795T>A
ENST00000673923.1:n.522T>A
ENST00000674147.1:c.2591T>A	ENSP00000500964.1:p.Ile864Asn
ENST00000242839.8:c.3656T>A	ENSP00000242839.4:p.Ile1219Asn
ENST00000344297.8:c.3035T>A	ENSP00000342559.5:p.Ile1012Asn
ENST00000400366.5:c.3323T>A	ENSP00000383217.3:p.Ile1108Asn
ENST00000400370.8:c.2366T>A	ENSP00000383221.3:p.Ile789Asn
ENST00000418097.7:c.3461T>A	ENSP00000393343.2:p.Ile1154Asn
ENST00000448424.6:c.3422T>A	ENSP00000416738.2:p.Ile1141Asn
ENST00000634296.1:c.1434T>A
ENST00000634308.1:c.*757T>A	ENSP00000489234.1:n.*757T>A
ENST00000634620.1:n.4400T>A
ENST00000634810.1:n.3001T>A
ENST00000634844.1:c.3512T>A	ENSP00000489398.1:p.Ile1171Asn
NM_000053.3:c.3656T>A	NP_000044.2:p.Ile1219Asn
NM_001005918.2:c.3035T>A	NP_001005918.1:p.Ile1012Asn
NM_001243182.1:c.3323T>A	NP_001230111.1:p.Ile1108Asn
XM_005266423.2:c.3560T>A	XP_005266480.1:p.Ile1187Asn
XM_005266424.3:c.3560T>A	XP_005266481.1:p.Ile1187Asn
XM_005266427.2:c.3422T>A	XP_005266484.1:p.Ile1141Asn
XM_005266428.1:c.3404T>A	XP_005266485.1:p.Ile1135Asn
XM_005266430.3:c.3656T>A	XP_005266487.1:p.Ile1219Asn
XM_005266431.2:c.3620T>A	XP_005266488.1:p.Ile1207Asn
XM_005266432.2:c.3170T>A	XP_005266489.1:p.Ile1057Asn
XM_006719837.2:c.3560T>A	XP_006719900.1:p.Ile1187Asn
XM_006719838.1:c.1472T>A	XP_006719901.1:p.Ile491Asn
XM_006719839.1:c.1289T>A	XP_006719902.1:p.Ile430Asn
XM_011535117.1:c.3560T>A	XP_011533419.1:p.Ile1187Asn
XM_011535118.1:c.3521T>A	XP_011533420.1:p.Ile1174Asn
XM_011535119.1:c.3473T>A	XP_011533421.1:p.Ile1158Asn
XM_011535120.1:c.3242T>A	XP_011533422.1:p.Ile1081Asn
XM_011535121.1:c.3143T>A	XP_011533423.1:p.Ile1048Asn
XM_011535122.1:c.2324T>A	XP_011533424.1:p.Ile775Asn
XR_941601.1:n.3875T>A
XR_941602.1:n.3875T>A
XR_941603.1:n.3875T>A
XR_941604.1:n.3875T>A
NM_001330578.1:c.3422T>A	NP_001317507.1:p.Ile1141Asn
NM_001330579.1:c.3404T>A	NP_001317508.1:p.Ile1135Asn
XM_005266424.4:c.3560T>A	XP_005266481.1:p.Ile1187Asn
XM_005266430.4:c.3656T>A	XP_005266487.1:p.Ile1219Asn
XM_005266431.4:c.3620T>A	XP_005266488.1:p.Ile1207Asn
XM_006719837.3:c.3560T>A	XP_006719900.1:p.Ile1187Asn
XM_011535117.3:c.3560T>A	XP_011533419.1:p.Ile1187Asn
XM_017020627.1:c.3560T>A	XP_016876116.1:p.Ile1187Asn
NM_000053.4:c.3656T>A MANE Select	NP_000044.2:p.Ile1219Asn
NM_001005918.3:c.3035T>A	NP_001005918.1:p.Ile1012Asn
NM_001330579.2:c.3404T>A	NP_001317508.1:p.Ile1135Asn
NM_001243182.2:c.3323T>A	NP_001230111.1:p.Ile1108Asn
NM_001330578.2:c.3422T>A	NP_001317507.1:p.Ile1141Asn