Canonical Allele Identifier: CA6884242

Gene: PUS1

Linked Data

• dbSNP Id: rs371146708
• ExAC: 12:132426074 G / A
• gnomAD v2: 12-132426074-G-A
• gnomAD v3: 12-131941529-G-A
• gnomAD v4: 12-131941529-G-A
• COSMIC: COSM3688059
• MyVariant Identifiers: chr12:g.132426074G>A (hg19) ; chr12:g.131941529G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941529G>A , CM000674.2:g.131941529G>A	GRCh38
NC_000012.11:g.132426074G>A , CM000674.1:g.132426074G>A	GRCh37
NC_000012.10:g.130992027G>A	NCBI36
NG_013039.1:g.17330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.782G>A MANE Select	ENSP00000365837.3:p.Arg261His
ENST00000322060.9:c.698G>A	ENSP00000324726.5:p.Arg233His
ENST00000376649.7:c.782G>A	ENSP00000365837.3:p.Arg261His
ENST00000443358.6:c.698G>A	ENSP00000392451.2:p.Arg233His
ENST00000535067.5:c.358-2010G>A	ENSP00000443969.1:n.358-2010G>A
ENST00000542167.2:c.623G>A	ENSP00000438948.1:p.Arg208His
ENST00000543754.1:n.603G>A
NM_001002019.2:c.698G>A	NP_001002019.1:p.Arg233His
NM_001002020.2:c.698G>A	NP_001002020.1:p.Arg233His
NM_025215.5:c.782G>A	NP_079491.2:p.Arg261His
XM_011538768.1:c.383G>A	XP_011537070.1:p.Arg128His
XM_011538768.3:c.383G>A	XP_011537070.1:p.Arg128His
XR_001748872.1:n.1237G>A
NM_001002019.3:c.698G>A	NP_001002019.1:p.Arg233His
NM_001002020.3:c.698G>A	NP_001002020.1:p.Arg233His
NM_025215.6:c.782G>A MANE Select	NP_079491.2:p.Arg261His