Canonical Allele Identifier: CA388021392

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52511622A>T (hg19) ; chr13:g.51937486A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51937486A>T , CM000675.2:g.51937486A>T	GRCh38
NC_000013.10:g.52511622A>T , CM000675.1:g.52511622A>T	GRCh37
NC_000013.9:g.51409623A>T	NCBI36
NG_008806.1:g.79009T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1543T>A	ENSP00000489512.2:n.*1543T>A
ENST00000673864.2:c.*2637T>A	ENSP00000501045.2:n.*2637T>A
ENST00000674147.2:c.3272T>A	ENSP00000500964.2:p.Val1091Asp
ENST00000242839.10:c.3893T>A MANE Select	ENSP00000242839.5:p.Val1298Asp
ENST00000344297.9:c.3272T>A	ENSP00000342559.5:p.Val1091Asp
ENST00000400366.6:c.3560T>A	ENSP00000383217.3:p.Val1187Asp
ENST00000448424.7:c.3641T>A	ENSP00000416738.3:p.Val1214Asp
ENST00000673696.1:n.1134T>A
ENST00000673772.1:c.3659T>A	ENSP00000501168.1:p.Val1220Asp
ENST00000673867.1:n.4032T>A
ENST00000673923.1:n.759T>A
ENST00000674147.1:c.2828T>A	ENSP00000500964.1:p.Val943Asp
ENST00000242839.8:c.3893T>A	ENSP00000242839.4:p.Val1298Asp
ENST00000344297.8:c.3272T>A	ENSP00000342559.5:p.Val1091Asp
ENST00000400366.5:c.3560T>A	ENSP00000383217.3:p.Val1187Asp
ENST00000400370.8:c.2603T>A	ENSP00000383221.3:p.Val868Asp
ENST00000418097.7:c.3698T>A	ENSP00000393343.2:p.Val1233Asp
ENST00000448424.6:c.3659T>A	ENSP00000416738.2:p.Val1220Asp
ENST00000634296.1:c.1671T>A
ENST00000634308.1:c.*994T>A	ENSP00000489234.1:n.*994T>A
ENST00000634620.1:n.4637T>A
ENST00000634810.1:n.3238T>A
ENST00000634844.1:c.3749T>A	ENSP00000489398.1:p.Val1250Asp
NM_000053.3:c.3893T>A	NP_000044.2:p.Val1298Asp
NM_001005918.2:c.3272T>A	NP_001005918.1:p.Val1091Asp
NM_001243182.1:c.3560T>A	NP_001230111.1:p.Val1187Asp
XM_005266423.2:c.3797T>A	XP_005266480.1:p.Val1266Asp
XM_005266424.3:c.3797T>A	XP_005266481.1:p.Val1266Asp
XM_005266427.2:c.3659T>A	XP_005266484.1:p.Val1220Asp
XM_005266428.1:c.3641T>A	XP_005266485.1:p.Val1214Asp
XM_005266430.3:c.3893T>A	XP_005266487.1:p.Val1298Asp
XM_005266431.2:c.3857T>A	XP_005266488.1:p.Val1286Asp
XM_005266432.2:c.3407T>A	XP_005266489.1:p.Val1136Asp
XM_006719837.2:c.3797T>A	XP_006719900.1:p.Val1266Asp
XM_006719838.1:c.1709T>A	XP_006719901.1:p.Val570Asp
XM_006719839.1:c.1526T>A	XP_006719902.1:p.Val509Asp
XM_011535117.1:c.3797T>A	XP_011533419.1:p.Val1266Asp
XM_011535118.1:c.3758T>A	XP_011533420.1:p.Val1253Asp
XM_011535119.1:c.3710T>A	XP_011533421.1:p.Val1237Asp
XM_011535120.1:c.3479T>A	XP_011533422.1:p.Val1160Asp
XM_011535121.1:c.3380T>A	XP_011533423.1:p.Val1127Asp
XM_011535122.1:c.2561T>A	XP_011533424.1:p.Val854Asp
XR_941601.1:n.4112T>A
XR_941602.1:n.4112T>A
XR_941603.1:n.4112T>A
XR_941604.1:n.4112T>A
NM_001330578.1:c.3659T>A	NP_001317507.1:p.Val1220Asp
NM_001330579.1:c.3641T>A	NP_001317508.1:p.Val1214Asp
XM_005266424.4:c.3797T>A	XP_005266481.1:p.Val1266Asp
XM_005266430.4:c.3893T>A	XP_005266487.1:p.Val1298Asp
XM_005266431.4:c.3857T>A	XP_005266488.1:p.Val1286Asp
XM_006719837.3:c.3797T>A	XP_006719900.1:p.Val1266Asp
XM_011535117.3:c.3797T>A	XP_011533419.1:p.Val1266Asp
XM_017020627.1:c.3797T>A	XP_016876116.1:p.Val1266Asp
NM_000053.4:c.3893T>A MANE Select	NP_000044.2:p.Val1298Asp
NM_001005918.3:c.3272T>A	NP_001005918.1:p.Val1091Asp
NM_001330579.2:c.3641T>A	NP_001317508.1:p.Val1214Asp
NM_001243182.2:c.3560T>A	NP_001230111.1:p.Val1187Asp
NM_001330578.2:c.3659T>A	NP_001317507.1:p.Val1220Asp