Canonical Allele Identifier: CA482841962

Gene: PUS1

Linked Data

• dbSNP Id: rs1254114259
• gnomAD v3: 12-131941404-T-C
• gnomAD v4: 12-131941404-T-C
• MyVariant Identifiers: chr12:g.132425949T>C (hg19) ; chr12:g.131941404T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941404T>C , CM000674.2:g.131941404T>C	GRCh38
NC_000012.11:g.132425949T>C , CM000674.1:g.132425949T>C	GRCh37
NC_000012.10:g.130991902T>C	NCBI36
NG_013039.1:g.17205T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.657T>C MANE Select	ENSP00000365837.3:p.Asp219=
ENST00000322060.9:c.573T>C	ENSP00000324726.5:p.Asp191=
ENST00000376649.7:c.657T>C	ENSP00000365837.3:p.Asp219=
ENST00000443358.6:c.573T>C	ENSP00000392451.2:p.Asp191=
ENST00000535067.5:c.358-2135T>C	ENSP00000443969.1:n.358-2135T>C
ENST00000537484.1:c.582T>C	ENSP00000440179.1:p.Asp194=
ENST00000542167.2:c.498T>C	ENSP00000438948.1:p.Asp166=
ENST00000543754.1:n.478T>C
NM_001002019.2:c.573T>C	NP_001002019.1:p.Asp191=
NM_001002020.2:c.573T>C	NP_001002020.1:p.Asp191=
NM_025215.5:c.657T>C	NP_079491.2:p.Asp219=
XM_011538768.1:c.258T>C	XP_011537070.1:p.Asp86=
XM_011538768.3:c.258T>C	XP_011537070.1:p.Asp86=
XR_001748872.1:n.1112T>C
NM_001002019.3:c.573T>C	NP_001002019.1:p.Asp191=
NM_001002020.3:c.573T>C	NP_001002020.1:p.Asp191=
NM_025215.6:c.657T>C MANE Select	NP_079491.2:p.Asp219=