Canonical Allele Identifier: CA388032480

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520583A>G (hg19) ; chr13:g.51946447A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946447A>G , CM000675.2:g.51946447A>G	GRCh38
NC_000013.10:g.52520583A>G , CM000675.1:g.52520583A>G	GRCh37
NC_000013.9:g.51418584A>G	NCBI36
NG_008806.1:g.70048T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*730T>C	ENSP00000489512.2:n.*730T>C
ENST00000673864.2:c.*1641T>C	ENSP00000501045.2:n.*1641T>C
ENST00000674147.2:c.2276T>C	ENSP00000500964.2:p.Val759Ala
ENST00000242839.10:c.2897T>C MANE Select	ENSP00000242839.5:p.Val966Ala
ENST00000344297.9:c.2276T>C	ENSP00000342559.5:p.Val759Ala
ENST00000400366.6:c.2564T>C	ENSP00000383217.3:p.Val855Ala
ENST00000448424.7:c.2645T>C	ENSP00000416738.3:p.Val882Ala
ENST00000673772.1:c.2663T>C	ENSP00000501168.1:p.Val888Ala
ENST00000673867.1:n.1044T>C
ENST00000674126.1:n.3260T>C
ENST00000674147.1:c.1832T>C	ENSP00000500964.1:p.Val611Ala
ENST00000242839.8:c.2897T>C	ENSP00000242839.4:p.Val966Ala
ENST00000344297.8:c.2276T>C	ENSP00000342559.5:p.Val759Ala
ENST00000400366.5:c.2564T>C	ENSP00000383217.3:p.Val855Ala
ENST00000400370.8:c.1607T>C	ENSP00000383221.3:p.Val536Ala
ENST00000418097.7:c.2866-2156T>C	ENSP00000393343.2:n.2866-2156T>C
ENST00000448424.6:c.2663T>C	ENSP00000416738.2:p.Val888Ala
ENST00000466629.1:n.117T>C
ENST00000634296.1:c.858T>C
ENST00000634308.1:c.2683T>C	ENSP00000489234.1:p.Ter895Arg
ENST00000634620.1:n.3641T>C
ENST00000634810.1:n.2242T>C
ENST00000634844.1:c.2753T>C	ENSP00000489398.1:p.Val918Ala
ENST00000635406.1:n.243T>C
NM_000053.3:c.2897T>C	NP_000044.2:p.Val966Ala
NM_001005918.2:c.2276T>C	NP_001005918.1:p.Val759Ala
NM_001243182.1:c.2564T>C	NP_001230111.1:p.Val855Ala
XM_005266423.2:c.2801T>C	XP_005266480.1:p.Val934Ala
XM_005266424.3:c.2801T>C	XP_005266481.1:p.Val934Ala
XM_005266427.2:c.2663T>C	XP_005266484.1:p.Val888Ala
XM_005266428.1:c.2645T>C	XP_005266485.1:p.Val882Ala
XM_005266430.3:c.2897T>C	XP_005266487.1:p.Val966Ala
XM_005266431.2:c.2861T>C	XP_005266488.1:p.Val954Ala
XM_005266432.2:c.2411T>C	XP_005266489.1:p.Val804Ala
XM_006719837.2:c.2801T>C	XP_006719900.1:p.Val934Ala
XM_006719838.1:c.713T>C	XP_006719901.1:p.Val238Ala
XM_006719839.1:c.713T>C	XP_006719902.1:p.Val238Ala
XM_011535117.1:c.2801T>C	XP_011533419.1:p.Val934Ala
XM_011535118.1:c.2762T>C	XP_011533420.1:p.Val921Ala
XM_011535119.1:c.2897T>C	XP_011533421.1:p.Val966Ala
XM_011535120.1:c.2483T>C	XP_011533422.1:p.Val828Ala
XM_011535121.1:c.2730+3560T>C	XP_011533423.1:n.2730+3560T>C
XM_011535122.1:c.1565T>C	XP_011533424.1:p.Val522Ala
XR_941601.1:n.3116T>C
XR_941602.1:n.3116T>C
XR_941603.1:n.3116T>C
XR_941604.1:n.3116T>C
NM_001330578.1:c.2663T>C	NP_001317507.1:p.Val888Ala
NM_001330579.1:c.2645T>C	NP_001317508.1:p.Val882Ala
XM_005266424.4:c.2801T>C	XP_005266481.1:p.Val934Ala
XM_005266430.4:c.2897T>C	XP_005266487.1:p.Val966Ala
XM_005266431.4:c.2861T>C	XP_005266488.1:p.Val954Ala
XM_006719837.3:c.2801T>C	XP_006719900.1:p.Val934Ala
XM_011535117.3:c.2801T>C	XP_011533419.1:p.Val934Ala
XM_017020627.1:c.2801T>C	XP_016876116.1:p.Val934Ala
NM_000053.4:c.2897T>C MANE Select	NP_000044.2:p.Val966Ala
NM_001005918.3:c.2276T>C	NP_001005918.1:p.Val759Ala
NM_001330579.2:c.2645T>C	NP_001317508.1:p.Val882Ala
NM_001243182.2:c.2564T>C	NP_001230111.1:p.Val855Ala
NM_001330578.2:c.2663T>C	NP_001317507.1:p.Val888Ala