Canonical Allele Identifier: CA2697551889

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 2758685
• ClinVar RCV Id: RCV003503161

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51960330G>T , CM000675.2:g.51960330G>T	GRCh38
NC_000013.10:g.52534466G>T , CM000675.1:g.52534466G>T	GRCh37
NC_000013.9:g.51432467G>T	NCBI36
NG_008806.1:g.56165C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.1946+1507C>A	ENSP00000489512.2:n.1946+1507C>A
ENST00000673864.2:c.*691-8C>A	ENSP00000501045.2:n.*691-8C>A
ENST00000674147.2:c.1870-2723C>A	ENSP00000500964.2:n.1870-2723C>A
ENST00000242839.10:c.1947-8C>A MANE Select	ENSP00000242839.5:n.1947-8C>A
ENST00000344297.9:c.1870-2723C>A	ENSP00000342559.5:n.1870-2723C>A
ENST00000400366.6:c.1614-8C>A	ENSP00000383217.3:n.1614-8C>A
ENST00000448424.7:c.1870-1786C>A	ENSP00000416738.3:n.1870-1786C>A
ENST00000673772.1:c.1947-8C>A	ENSP00000501168.1:n.1947-8C>A
ENST00000674147.1:c.1426-2723C>A	ENSP00000500964.1:n.1426-2723C>A
ENST00000242839.8:c.1947-8C>A	ENSP00000242839.4:n.1947-8C>A
ENST00000344297.8:c.1870-2723C>A	ENSP00000342559.5:n.1870-2723C>A
ENST00000400366.5:c.1614-8C>A	ENSP00000383217.3:n.1614-8C>A
ENST00000400370.8:c.1286-10169C>A	ENSP00000383221.3:n.1286-10169C>A
ENST00000418097.7:c.1947-8C>A	ENSP00000393343.2:n.1947-8C>A
ENST00000448424.6:c.1947-8C>A	ENSP00000416738.2:n.1947-8C>A
ENST00000482841.6:n.1665-1786C>A
ENST00000634296.1:c.82+1507C>A
ENST00000634308.1:c.1947-8C>A	ENSP00000489234.1:n.1947-8C>A
ENST00000634620.1:n.439-8C>A
ENST00000634844.1:c.1947-8C>A	ENSP00000489398.1:n.1947-8C>A
ENST00000635406.1:n.212-13852C>A
NM_000053.3:c.1947-8C>A	NP_000044.2:n.1947-8C>A
NM_001005918.2:c.1870-2723C>A	NP_001005918.1:n.1870-2723C>A
NM_001243182.1:c.1614-8C>A	NP_001230111.1:n.1614-8C>A
XM_005266423.2:c.1851-8C>A	XP_005266480.1:n.1851-8C>A
XM_005266424.3:c.1851-8C>A	XP_005266481.1:n.1851-8C>A
XM_005266427.2:c.1947-8C>A	XP_005266484.1:n.1947-8C>A
XM_005266428.1:c.1870-1786C>A	XP_005266485.1:n.1870-1786C>A
XM_005266430.3:c.1947-8C>A	XP_005266487.1:n.1947-8C>A
XM_005266431.2:c.1911-8C>A	XP_005266488.1:n.1911-8C>A
XM_005266432.2:c.1870-2723C>A	XP_005266489.1:n.1870-2723C>A
XM_006719837.2:c.1851-8C>A	XP_006719900.1:n.1851-8C>A
XM_006719838.1:c.-64+1507C>A	XP_006719901.1:n.-64+1507C>A
XM_006719839.1:c.-64+1507C>A	XP_006719902.1:n.-64+1507C>A
XM_011535117.1:c.1851-8C>A	XP_011533419.1:n.1851-8C>A
XM_011535118.1:c.1947-8C>A	XP_011533420.1:n.1947-8C>A
XM_011535119.1:c.1947-8C>A	XP_011533421.1:n.1947-8C>A
XM_011535120.1:c.1708-1786C>A	XP_011533422.1:n.1708-1786C>A
XM_011535121.1:c.1947-8C>A	XP_011533423.1:n.1947-8C>A
XM_011535122.1:c.615-8C>A	XP_011533424.1:n.615-8C>A
XR_941601.1:n.2166-8C>A
XR_941602.1:n.2166-8C>A
XR_941603.1:n.2166-8C>A
XR_941604.1:n.2166-8C>A
NM_001330578.1:c.1947-8C>A	NP_001317507.1:n.1947-8C>A
NM_001330579.1:c.1870-1786C>A	NP_001317508.1:n.1870-1786C>A
XM_005266424.4:c.1851-8C>A	XP_005266481.1:n.1851-8C>A
XM_005266430.4:c.1947-8C>A	XP_005266487.1:n.1947-8C>A
XM_005266431.4:c.1911-8C>A	XP_005266488.1:n.1911-8C>A
XM_006719837.3:c.1851-8C>A	XP_006719900.1:n.1851-8C>A
XM_011535117.3:c.1851-8C>A	XP_011533419.1:n.1851-8C>A
XM_017020627.1:c.1851-8C>A	XP_016876116.1:n.1851-8C>A
NM_000053.4:c.1947-8C>A MANE Select	NP_000044.2:n.1947-8C>A
NM_001005918.3:c.1870-2723C>A	NP_001005918.1:n.1870-2723C>A
NM_001330579.2:c.1870-1786C>A	NP_001317508.1:n.1870-1786C>A
NM_001243182.2:c.1614-8C>A	NP_001230111.1:n.1614-8C>A
NM_001330578.2:c.1947-8C>A	NP_001317507.1:n.1947-8C>A