Canonical Allele Identifier: CA246187224

Gene: PUS1

Linked Data

• dbSNP Id: rs376412844
• gnomAD v3: 12-131941522-G-A
• gnomAD v4: 12-131941522-G-A
• MyVariant Identifiers: chr12:g.132426067G>A (hg19) ; chr12:g.131941522G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941522G>A , CM000674.2:g.131941522G>A	GRCh38
NC_000012.11:g.132426067G>A , CM000674.1:g.132426067G>A	GRCh37
NC_000012.10:g.130992020G>A	NCBI36
NG_013039.1:g.17323G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.775G>A MANE Select	ENSP00000365837.3:p.Ala259Thr
ENST00000322060.9:c.691G>A	ENSP00000324726.5:p.Ala231Thr
ENST00000376649.7:c.775G>A	ENSP00000365837.3:p.Ala259Thr
ENST00000443358.6:c.691G>A	ENSP00000392451.2:p.Ala231Thr
ENST00000535067.5:c.358-2017G>A	ENSP00000443969.1:n.358-2017G>A
ENST00000542167.2:c.616G>A	ENSP00000438948.1:p.Ala206Thr
ENST00000543754.1:n.596G>A
NM_001002019.2:c.691G>A	NP_001002019.1:p.Ala231Thr
NM_001002020.2:c.691G>A	NP_001002020.1:p.Ala231Thr
NM_025215.5:c.775G>A	NP_079491.2:p.Ala259Thr
XM_011538768.1:c.376G>A	XP_011537070.1:p.Ala126Thr
XM_011538768.3:c.376G>A	XP_011537070.1:p.Ala126Thr
XR_001748872.1:n.1230G>A
NM_001002019.3:c.691G>A	NP_001002019.1:p.Ala231Thr
NM_001002020.3:c.691G>A	NP_001002020.1:p.Ala231Thr
NM_025215.6:c.775G>A MANE Select	NP_079491.2:p.Ala259Thr