Canonical Allele Identifier: CA482841646

Gene: PUS1

Linked Data

• gnomAD v4: 12-131941329-C-T
• MyVariant Identifiers: chr12:g.132425874C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941329C>T , CM000674.2:g.131941329C>T	GRCh38
NC_000012.11:g.132425874C>T , CM000674.1:g.132425874C>T	GRCh37
NC_000012.10:g.130991827C>T	NCBI36
NG_013039.1:g.17130C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.582C>T MANE Select	ENSP00000365837.3:p.Asn194=
ENST00000322060.9:c.498C>T	ENSP00000324726.5:p.Asn166=
ENST00000376649.7:c.582C>T	ENSP00000365837.3:p.Asn194=
ENST00000443358.6:c.498C>T	ENSP00000392451.2:p.Asn166=
ENST00000535067.5:c.358-2210C>T	ENSP00000443969.1:n.358-2210C>T
ENST00000537484.1:c.507C>T	ENSP00000440179.1:p.Asn169=
ENST00000542167.2:c.423C>T	ENSP00000438948.1:p.Asn141=
ENST00000543754.1:n.403C>T
NM_001002019.2:c.498C>T	NP_001002019.1:p.Asn166=
NM_001002020.2:c.498C>T	NP_001002020.1:p.Asn166=
NM_025215.5:c.582C>T	NP_079491.2:p.Asn194=
XM_011538768.1:c.183C>T	XP_011537070.1:p.Asn61=
XM_011538768.3:c.183C>T	XP_011537070.1:p.Asn61=
XR_001748872.1:n.1037C>T
NM_001002019.3:c.498C>T	NP_001002019.1:p.Asn166=
NM_001002020.3:c.498C>T	NP_001002020.1:p.Asn166=
NM_025215.6:c.582C>T MANE Select	NP_079491.2:p.Asn194=