Canonical Allele Identifier: CA388026812

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 2475812
• ClinVar RCV Id: RCV003193265
• dbSNP Id: rs1957311959
• gnomAD v4: 13-51941219-C-T
• MyVariant Identifiers: chr13:g.52515355C>T (hg19) ; chr13:g.51941219C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941219C>T , CM000675.2:g.51941219C>T	GRCh38
NC_000013.10:g.52515355C>T , CM000675.1:g.52515355C>T	GRCh37
NC_000013.9:g.51413356C>T	NCBI36
NG_008806.1:g.75276G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1068G>A	ENSP00000489512.2:n.*1068G>A
ENST00000673864.2:c.*2162G>A	ENSP00000501045.2:n.*2162G>A
ENST00000674147.2:c.2797G>A	ENSP00000500964.2:p.Val933Ile
ENST00000242839.10:c.3418G>A MANE Select	ENSP00000242839.5:p.Val1140Ile
ENST00000344297.9:c.2797G>A	ENSP00000342559.5:p.Val933Ile
ENST00000400366.6:c.3085G>A	ENSP00000383217.3:p.Val1029Ile
ENST00000448424.7:c.3166G>A	ENSP00000416738.3:p.Val1056Ile
ENST00000673772.1:c.3184G>A	ENSP00000501168.1:p.Val1062Ile
ENST00000673867.1:n.3557G>A
ENST00000674126.1:n.3781G>A
ENST00000674147.1:c.2353G>A	ENSP00000500964.1:p.Val785Ile
ENST00000242839.8:c.3418G>A	ENSP00000242839.4:p.Val1140Ile
ENST00000344297.8:c.2797G>A	ENSP00000342559.5:p.Val933Ile
ENST00000400366.5:c.3085G>A	ENSP00000383217.3:p.Val1029Ile
ENST00000400370.8:c.2128G>A	ENSP00000383221.3:p.Val710Ile
ENST00000418097.7:c.3223G>A	ENSP00000393343.2:p.Val1075Ile
ENST00000448424.6:c.3184G>A	ENSP00000416738.2:p.Val1062Ile
ENST00000634296.1:c.1196G>A
ENST00000634308.1:c.*519G>A	ENSP00000489234.1:n.*519G>A
ENST00000634620.1:n.4162G>A
ENST00000634810.1:n.2763G>A
ENST00000634844.1:c.3274G>A	ENSP00000489398.1:p.Val1092Ile
NM_000053.3:c.3418G>A	NP_000044.2:p.Val1140Ile
NM_001005918.2:c.2797G>A	NP_001005918.1:p.Val933Ile
NM_001243182.1:c.3085G>A	NP_001230111.1:p.Val1029Ile
XM_005266423.2:c.3322G>A	XP_005266480.1:p.Val1108Ile
XM_005266424.3:c.3322G>A	XP_005266481.1:p.Val1108Ile
XM_005266427.2:c.3184G>A	XP_005266484.1:p.Val1062Ile
XM_005266428.1:c.3166G>A	XP_005266485.1:p.Val1056Ile
XM_005266430.3:c.3418G>A	XP_005266487.1:p.Val1140Ile
XM_005266431.2:c.3382G>A	XP_005266488.1:p.Val1128Ile
XM_005266432.2:c.2932G>A	XP_005266489.1:p.Val978Ile
XM_006719837.2:c.3322G>A	XP_006719900.1:p.Val1108Ile
XM_006719838.1:c.1234G>A	XP_006719901.1:p.Val412Ile
XM_006719839.1:c.1051G>A	XP_006719902.1:p.Val351Ile
XM_011535117.1:c.3322G>A	XP_011533419.1:p.Val1108Ile
XM_011535118.1:c.3283G>A	XP_011533420.1:p.Val1095Ile
XM_011535119.1:c.3235G>A	XP_011533421.1:p.Val1079Ile
XM_011535120.1:c.3004G>A	XP_011533422.1:p.Val1002Ile
XM_011535121.1:c.2905G>A	XP_011533423.1:p.Val969Ile
XM_011535122.1:c.2086G>A	XP_011533424.1:p.Val696Ile
XR_941601.1:n.3637G>A
XR_941602.1:n.3637G>A
XR_941603.1:n.3637G>A
XR_941604.1:n.3637G>A
NM_001330578.1:c.3184G>A	NP_001317507.1:p.Val1062Ile
NM_001330579.1:c.3166G>A	NP_001317508.1:p.Val1056Ile
XM_005266424.4:c.3322G>A	XP_005266481.1:p.Val1108Ile
XM_005266430.4:c.3418G>A	XP_005266487.1:p.Val1140Ile
XM_005266431.4:c.3382G>A	XP_005266488.1:p.Val1128Ile
XM_006719837.3:c.3322G>A	XP_006719900.1:p.Val1108Ile
XM_011535117.3:c.3322G>A	XP_011533419.1:p.Val1108Ile
XM_017020627.1:c.3322G>A	XP_016876116.1:p.Val1108Ile
NM_000053.4:c.3418G>A MANE Select	NP_000044.2:p.Val1140Ile
NM_001005918.3:c.2797G>A	NP_001005918.1:p.Val933Ile
NM_001330579.2:c.3166G>A	NP_001317508.1:p.Val1056Ile
NM_001243182.2:c.3085G>A	NP_001230111.1:p.Val1029Ile
NM_001330578.2:c.3184G>A	NP_001317507.1:p.Val1062Ile