Canonical Allele Identifier: CA482841635

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132425865C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941320C>T , CM000674.2:g.131941320C>T	GRCh38
NC_000012.11:g.132425865C>T , CM000674.1:g.132425865C>T	GRCh37
NC_000012.10:g.130991818C>T	NCBI36
NG_013039.1:g.17121C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.573C>T MANE Select	ENSP00000365837.3:p.Asn191=
ENST00000322060.9:c.489C>T	ENSP00000324726.5:p.Asn163=
ENST00000376649.7:c.573C>T	ENSP00000365837.3:p.Asn191=
ENST00000443358.6:c.489C>T	ENSP00000392451.2:p.Asn163=
ENST00000535067.5:c.358-2219C>T	ENSP00000443969.1:n.358-2219C>T
ENST00000537484.1:c.498C>T	ENSP00000440179.1:p.Asn166=
ENST00000542167.2:c.414C>T	ENSP00000438948.1:p.Asn138=
ENST00000543754.1:n.394C>T
NM_001002019.2:c.489C>T	NP_001002019.1:p.Asn163=
NM_001002020.2:c.489C>T	NP_001002020.1:p.Asn163=
NM_025215.5:c.573C>T	NP_079491.2:p.Asn191=
XM_011538768.1:c.174C>T	XP_011537070.1:p.Asn58=
XM_011538768.3:c.174C>T	XP_011537070.1:p.Asn58=
XR_001748872.1:n.1028C>T
NM_001002019.3:c.489C>T	NP_001002019.1:p.Asn163=
NM_001002020.3:c.489C>T	NP_001002020.1:p.Asn163=
NM_025215.6:c.573C>T MANE Select	NP_079491.2:p.Asn191=