Canonical Allele Identifier: CA6989325

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 2912657
• ClinVar RCV Id: RCV003609814
• dbSNP Id: rs768330277
• ExAC: 13:52544609 ATG / A
• gnomAD v3: 13-51970473-ATG-A
• gnomAD v4: 13-51970473-ATG-A
• MyVariant Identifiers: chr13:g.52544610_52544611del (hg19) ; chr13:g.51970474_51970475del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51970474_51970475del , CM000675.2:g.51970474_51970475del	GRCh38
NC_000013.10:g.52544610_52544611del , CM000675.1:g.52544610_52544611del	GRCh37
NC_000013.9:g.51442611_51442612del	NCBI36
NG_008806.1:g.46020_46021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.1543+17_1543+18del	ENSP00000489512.2:n.1543+17_1543+18del
ENST00000673864.2:c.*287+17_*287+18del	ENSP00000501045.2:n.*287+17_*287+18del
ENST00000674147.2:c.1543+17_1543+18del	ENSP00000500964.2:n.1543+17_1543+18del
ENST00000242839.10:c.1543+17_1543+18del MANE Select	ENSP00000242839.5:n.1543+17_1543+18del
ENST00000344297.9:c.1543+17_1543+18del	ENSP00000342559.5:n.1543+17_1543+18del
ENST00000400366.6:c.1210+17_1210+18del	ENSP00000383217.3:n.1210+17_1210+18del
ENST00000448424.7:c.1543+17_1543+18del	ENSP00000416738.3:n.1543+17_1543+18del
ENST00000483772.2:n.299+17_299+18del
ENST00000673772.1:c.1543+17_1543+18del	ENSP00000501168.1:n.1543+17_1543+18del
ENST00000673789.1:n.499+17_499+18del
ENST00000673864.1:c.737+17_737+18del	ENSP00000501045.1:n.737+17_737+18del
ENST00000674078.1:n.1661_1662del
ENST00000674147.1:c.1099+17_1099+18del	ENSP00000500964.1:n.1099+17_1099+18del
ENST00000242839.8:c.1543+17_1543+18del	ENSP00000242839.4:n.1543+17_1543+18del
ENST00000344297.8:c.1543+17_1543+18del	ENSP00000342559.5:n.1543+17_1543+18del
ENST00000400366.5:c.1210+17_1210+18del	ENSP00000383217.3:n.1210+17_1210+18del
ENST00000400370.8:c.1285+3460_1285+3461del	ENSP00000383221.3:n.1285+3460_1285+3461del
ENST00000418097.7:c.1543+17_1543+18del	ENSP00000393343.2:n.1543+17_1543+18del
ENST00000448424.6:c.1543+17_1543+18del	ENSP00000416738.2:n.1543+17_1543+18del
ENST00000482841.6:n.1664+17_1664+18del
ENST00000483772.1:n.299+17_299+18del
ENST00000634308.1:c.1543+17_1543+18del	ENSP00000489234.1:n.1543+17_1543+18del
ENST00000634620.1:n.35+17_35+18del
ENST00000634844.1:c.1543+17_1543+18del	ENSP00000489398.1:n.1543+17_1543+18del
ENST00000635406.1:n.212-23997_212-23996del
NM_000053.3:c.1543+17_1543+18del	NP_000044.2:n.1543+17_1543+18del
NM_001005918.2:c.1543+17_1543+18del	NP_001005918.1:n.1543+17_1543+18del
NM_001243182.1:c.1210+17_1210+18del	NP_001230111.1:n.1210+17_1210+18del
XM_005266423.2:c.1447+17_1447+18del	XP_005266480.1:n.1447+17_1447+18del
XM_005266424.3:c.1447+17_1447+18del	XP_005266481.1:n.1447+17_1447+18del
XM_005266427.2:c.1543+17_1543+18del	XP_005266484.1:n.1543+17_1543+18del
XM_005266428.1:c.1543+17_1543+18del	XP_005266485.1:n.1543+17_1543+18del
XM_005266430.3:c.1543+17_1543+18del	XP_005266487.1:n.1543+17_1543+18del
XM_005266431.2:c.1507+17_1507+18del	XP_005266488.1:n.1507+17_1507+18del
XM_005266432.2:c.1543+17_1543+18del	XP_005266489.1:n.1543+17_1543+18del
XM_006719837.2:c.1447+17_1447+18del	XP_006719900.1:n.1447+17_1447+18del
XM_011535117.1:c.1447+17_1447+18del	XP_011533419.1:n.1447+17_1447+18del
XM_011535118.1:c.1543+17_1543+18del	XP_011533420.1:n.1543+17_1543+18del
XM_011535119.1:c.1543+17_1543+18del	XP_011533421.1:n.1543+17_1543+18del
XM_011535120.1:c.1543+17_1543+18del	XP_011533422.1:n.1543+17_1543+18del
XM_011535121.1:c.1543+17_1543+18del	XP_011533423.1:n.1543+17_1543+18del
XM_011535122.1:c.211+17_211+18del	XP_011533424.1:n.211+17_211+18del
XR_941601.1:n.1762+17_1762+18del
XR_941602.1:n.1762+17_1762+18del
XR_941603.1:n.1762+17_1762+18del
XR_941604.1:n.1762+17_1762+18del
NM_001330578.1:c.1543+17_1543+18del	NP_001317507.1:n.1543+17_1543+18del
NM_001330579.1:c.1543+17_1543+18del	NP_001317508.1:n.1543+17_1543+18del
XM_005266424.4:c.1447+17_1447+18del	XP_005266481.1:n.1447+17_1447+18del
XM_005266430.4:c.1543+17_1543+18del	XP_005266487.1:n.1543+17_1543+18del
XM_005266431.4:c.1507+17_1507+18del	XP_005266488.1:n.1507+17_1507+18del
XM_006719837.3:c.1447+17_1447+18del	XP_006719900.1:n.1447+17_1447+18del
XM_011535117.3:c.1447+17_1447+18del	XP_011533419.1:n.1447+17_1447+18del
XM_017020627.1:c.1447+17_1447+18del	XP_016876116.1:n.1447+17_1447+18del
NM_000053.4:c.1543+17_1543+18del MANE Select	NP_000044.2:n.1543+17_1543+18del
NM_001005918.3:c.1543+17_1543+18del	NP_001005918.1:n.1543+17_1543+18del
NM_001330579.2:c.1543+17_1543+18del	NP_001317508.1:n.1543+17_1543+18del
NM_001243182.2:c.1210+17_1210+18del	NP_001230111.1:n.1210+17_1210+18del
NM_001330578.2:c.1543+17_1543+18del	NP_001317507.1:n.1543+17_1543+18del