Canonical Allele Identifier: CA482842203

Gene: PUS1

Linked Data

• ClinVar Variation Id: 2775820
• ClinVar RCV Id: RCV003662770
• gnomAD v4: 12-131941527-C-T
• COSMIC: COSM4040224
• MyVariant Identifiers: chr12:g.132426072C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941527C>T , CM000674.2:g.131941527C>T	GRCh38
NC_000012.11:g.132426072C>T , CM000674.1:g.132426072C>T	GRCh37
NC_000012.10:g.130992025C>T	NCBI36
NG_013039.1:g.17328C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.780C>T MANE Select	ENSP00000365837.3:p.Cys260=
ENST00000322060.9:c.696C>T	ENSP00000324726.5:p.Cys232=
ENST00000376649.7:c.780C>T	ENSP00000365837.3:p.Cys260=
ENST00000443358.6:c.696C>T	ENSP00000392451.2:p.Cys232=
ENST00000535067.5:c.358-2012C>T	ENSP00000443969.1:n.358-2012C>T
ENST00000542167.2:c.621C>T	ENSP00000438948.1:p.Cys207=
ENST00000543754.1:n.601C>T
NM_001002019.2:c.696C>T	NP_001002019.1:p.Cys232=
NM_001002020.2:c.696C>T	NP_001002020.1:p.Cys232=
NM_025215.5:c.780C>T	NP_079491.2:p.Cys260=
XM_011538768.1:c.381C>T	XP_011537070.1:p.Cys127=
XM_011538768.3:c.381C>T	XP_011537070.1:p.Cys127=
XR_001748872.1:n.1235C>T
NM_001002019.3:c.696C>T	NP_001002019.1:p.Cys232=
NM_001002020.3:c.696C>T	NP_001002020.1:p.Cys232=
NM_025215.6:c.780C>T MANE Select	NP_079491.2:p.Cys260=