Canonical Allele Identifier: CA388024535

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513300C>T (hg19) ; chr13:g.51939164C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939164C>T , CM000675.2:g.51939164C>T	GRCh38
NC_000013.10:g.52513300C>T , CM000675.1:g.52513300C>T	GRCh37
NC_000013.9:g.51411301C>T	NCBI36
NG_008806.1:g.77331G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1236G>A	ENSP00000489512.2:n.*1236G>A
ENST00000673864.2:c.*2330G>A	ENSP00000501045.2:n.*2330G>A
ENST00000674147.2:c.2965G>A	ENSP00000500964.2:p.Asp989Asn
ENST00000242839.10:c.3586G>A MANE Select	ENSP00000242839.5:p.Asp1196Asn
ENST00000344297.9:c.2965G>A	ENSP00000342559.5:p.Asp989Asn
ENST00000400366.6:c.3253G>A	ENSP00000383217.3:p.Asp1085Asn
ENST00000448424.7:c.3334G>A	ENSP00000416738.3:p.Asp1112Asn
ENST00000673696.1:n.827G>A
ENST00000673772.1:c.3352G>A	ENSP00000501168.1:p.Asp1118Asn
ENST00000673867.1:n.3725G>A
ENST00000673923.1:n.452G>A
ENST00000674147.1:c.2521G>A	ENSP00000500964.1:p.Asp841Asn
ENST00000242839.8:c.3586G>A	ENSP00000242839.4:p.Asp1196Asn
ENST00000344297.8:c.2965G>A	ENSP00000342559.5:p.Asp989Asn
ENST00000400366.5:c.3253G>A	ENSP00000383217.3:p.Asp1085Asn
ENST00000400370.8:c.2296G>A	ENSP00000383221.3:p.Asp766Asn
ENST00000418097.7:c.3391G>A	ENSP00000393343.2:p.Asp1131Asn
ENST00000448424.6:c.3352G>A	ENSP00000416738.2:p.Asp1118Asn
ENST00000634296.1:c.1364G>A
ENST00000634308.1:c.*687G>A	ENSP00000489234.1:n.*687G>A
ENST00000634620.1:n.4330G>A
ENST00000634810.1:n.2931G>A
ENST00000634844.1:c.3442G>A	ENSP00000489398.1:p.Asp1148Asn
NM_000053.3:c.3586G>A	NP_000044.2:p.Asp1196Asn
NM_001005918.2:c.2965G>A	NP_001005918.1:p.Asp989Asn
NM_001243182.1:c.3253G>A	NP_001230111.1:p.Asp1085Asn
XM_005266423.2:c.3490G>A	XP_005266480.1:p.Asp1164Asn
XM_005266424.3:c.3490G>A	XP_005266481.1:p.Asp1164Asn
XM_005266427.2:c.3352G>A	XP_005266484.1:p.Asp1118Asn
XM_005266428.1:c.3334G>A	XP_005266485.1:p.Asp1112Asn
XM_005266430.3:c.3586G>A	XP_005266487.1:p.Asp1196Asn
XM_005266431.2:c.3550G>A	XP_005266488.1:p.Asp1184Asn
XM_005266432.2:c.3100G>A	XP_005266489.1:p.Asp1034Asn
XM_006719837.2:c.3490G>A	XP_006719900.1:p.Asp1164Asn
XM_006719838.1:c.1402G>A	XP_006719901.1:p.Asp468Asn
XM_006719839.1:c.1219G>A	XP_006719902.1:p.Asp407Asn
XM_011535117.1:c.3490G>A	XP_011533419.1:p.Asp1164Asn
XM_011535118.1:c.3451G>A	XP_011533420.1:p.Asp1151Asn
XM_011535119.1:c.3403G>A	XP_011533421.1:p.Asp1135Asn
XM_011535120.1:c.3172G>A	XP_011533422.1:p.Asp1058Asn
XM_011535121.1:c.3073G>A	XP_011533423.1:p.Asp1025Asn
XM_011535122.1:c.2254G>A	XP_011533424.1:p.Asp752Asn
XR_941601.1:n.3805G>A
XR_941602.1:n.3805G>A
XR_941603.1:n.3805G>A
XR_941604.1:n.3805G>A
NM_001330578.1:c.3352G>A	NP_001317507.1:p.Asp1118Asn
NM_001330579.1:c.3334G>A	NP_001317508.1:p.Asp1112Asn
XM_005266424.4:c.3490G>A	XP_005266481.1:p.Asp1164Asn
XM_005266430.4:c.3586G>A	XP_005266487.1:p.Asp1196Asn
XM_005266431.4:c.3550G>A	XP_005266488.1:p.Asp1184Asn
XM_006719837.3:c.3490G>A	XP_006719900.1:p.Asp1164Asn
XM_011535117.3:c.3490G>A	XP_011533419.1:p.Asp1164Asn
XM_017020627.1:c.3490G>A	XP_016876116.1:p.Asp1164Asn
NM_000053.4:c.3586G>A MANE Select	NP_000044.2:p.Asp1196Asn
NM_001005918.3:c.2965G>A	NP_001005918.1:p.Asp989Asn
NM_001330579.2:c.3334G>A	NP_001317508.1:p.Asp1112Asn
NM_001243182.2:c.3253G>A	NP_001230111.1:p.Asp1085Asn
NM_001330578.2:c.3352G>A	NP_001317507.1:p.Asp1118Asn