Canonical Allele Identifier: CA6988488

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 371170
• ClinVar RCV Id: RCV000411139
• dbSNP Id: rs755584106
• ExAC: 13:52509739 G / A
• gnomAD v2: 13-52509739-G-A
• gnomAD v4: 13-51935603-G-A
• COSMIC: COSM6406777
• MyVariant Identifiers: chr13:g.52509739G>A (hg19) ; chr13:g.51935603G>A (hg38)
• PubMed: PMID:21034864 ; PMID:25525159 ; PMID:27398169

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51935603G>A , CM000675.2:g.51935603G>A	GRCh38
NC_000013.10:g.52509739G>A , CM000675.1:g.52509739G>A	GRCh37
NC_000013.9:g.51407740G>A	NCBI36
NG_008806.1:g.80892C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1764C>T	ENSP00000489512.2:n.*1764C>T
ENST00000673864.2:c.*2858C>T	ENSP00000501045.2:n.*2858C>T
ENST00000674147.2:c.3493C>T	ENSP00000500964.2:p.Gln1165Ter
ENST00000242839.10:c.4114C>T MANE Select	ENSP00000242839.5:p.Gln1372Ter
ENST00000344297.9:c.3493C>T	ENSP00000342559.5:p.Gln1165Ter
ENST00000400366.6:c.3781C>T	ENSP00000383217.3:p.Gln1261Ter
ENST00000448424.7:c.3862C>T	ENSP00000416738.3:p.Gln1288Ter
ENST00000673696.1:n.1437C>T
ENST00000673772.1:c.3880C>T	ENSP00000501168.1:p.Gln1294Ter
ENST00000673867.1:n.4253C>T
ENST00000673923.1:n.980C>T
ENST00000674147.1:c.3049C>T	ENSP00000500964.1:p.Gln1017Ter
ENST00000242839.8:c.4114C>T	ENSP00000242839.4:p.Gln1372Ter
ENST00000344297.8:c.3493C>T	ENSP00000342559.5:p.Gln1165Ter
ENST00000400366.5:c.3781C>T	ENSP00000383217.3:p.Gln1261Ter
ENST00000400370.8:c.2824C>T	ENSP00000383221.3:p.Gln942Ter
ENST00000418097.7:c.3919C>T	ENSP00000393343.2:p.Gln1307Ter
ENST00000448424.6:c.3880C>T	ENSP00000416738.2:p.Gln1294Ter
ENST00000634296.1:c.1892C>T
ENST00000634308.1:c.*1215C>T	ENSP00000489234.1:n.*1215C>T
ENST00000634620.1:n.4858C>T
ENST00000634810.1:n.3459C>T
ENST00000634844.1:c.3970C>T	ENSP00000489398.1:p.Gln1324Ter
NM_000053.3:c.4114C>T	NP_000044.2:p.Gln1372Ter
NM_001005918.2:c.3493C>T	NP_001005918.1:p.Gln1165Ter
NM_001243182.1:c.3781C>T	NP_001230111.1:p.Gln1261Ter
XM_005266423.2:c.4018C>T	XP_005266480.1:p.Gln1340Ter
XM_005266424.3:c.4018C>T	XP_005266481.1:p.Gln1340Ter
XM_005266427.2:c.3880C>T	XP_005266484.1:p.Gln1294Ter
XM_005266428.1:c.3862C>T	XP_005266485.1:p.Gln1288Ter
XM_005266430.3:c.4114C>T	XP_005266487.1:p.Gln1372Ter
XM_005266431.2:c.4078C>T	XP_005266488.1:p.Gln1360Ter
XM_005266432.2:c.3628C>T	XP_005266489.1:p.Gln1210Ter
XM_006719837.2:c.4018C>T	XP_006719900.1:p.Gln1340Ter
XM_006719838.1:c.1930C>T	XP_006719901.1:p.Gln644Ter
XM_006719839.1:c.1747C>T	XP_006719902.1:p.Gln583Ter
XM_011535117.1:c.4018C>T	XP_011533419.1:p.Gln1340Ter
XM_011535118.1:c.3979C>T	XP_011533420.1:p.Gln1327Ter
XM_011535119.1:c.3931C>T	XP_011533421.1:p.Gln1311Ter
XM_011535120.1:c.3700C>T	XP_011533422.1:p.Gln1234Ter
XM_011535121.1:c.3601C>T	XP_011533423.1:p.Gln1201Ter
XM_011535122.1:c.2782C>T	XP_011533424.1:p.Gln928Ter
XR_941601.1:n.4333C>T
XR_941602.1:n.4333C>T
XR_941603.1:n.4333C>T
XR_941604.1:n.4333C>T
NM_001330578.1:c.3880C>T	NP_001317507.1:p.Gln1294Ter
NM_001330579.1:c.3862C>T	NP_001317508.1:p.Gln1288Ter
XM_005266424.4:c.4018C>T	XP_005266481.1:p.Gln1340Ter
XM_005266430.4:c.4114C>T	XP_005266487.1:p.Gln1372Ter
XM_005266431.4:c.4078C>T	XP_005266488.1:p.Gln1360Ter
XM_006719837.3:c.4018C>T	XP_006719900.1:p.Gln1340Ter
XM_011535117.3:c.4018C>T	XP_011533419.1:p.Gln1340Ter
XM_017020627.1:c.4018C>T	XP_016876116.1:p.Gln1340Ter
NM_000053.4:c.4114C>T MANE Select	NP_000044.2:p.Gln1372Ter
NM_001005918.3:c.3493C>T	NP_001005918.1:p.Gln1165Ter
NM_001330579.2:c.3862C>T	NP_001317508.1:p.Gln1288Ter
NM_001243182.2:c.3781C>T	NP_001230111.1:p.Gln1261Ter
NM_001330578.2:c.3880C>T	NP_001317507.1:p.Gln1294Ter