Canonical Allele Identifier: CA482841638

Gene: PUS1

Linked Data

• dbSNP Id: rs1215559539
• gnomAD v2: 12-132425868-C-T
• gnomAD v4: 12-131941323-C-T
• COSMIC: COSM5586362
• MyVariant Identifiers: chr12:g.132425868C>T (hg19) ; chr12:g.131941323C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941323C>T , CM000674.2:g.131941323C>T	GRCh38
NC_000012.11:g.132425868C>T , CM000674.1:g.132425868C>T	GRCh37
NC_000012.10:g.130991821C>T	NCBI36
NG_013039.1:g.17124C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.576C>T MANE Select	ENSP00000365837.3:p.Ser192=
ENST00000322060.9:c.492C>T	ENSP00000324726.5:p.Ser164=
ENST00000376649.7:c.576C>T	ENSP00000365837.3:p.Ser192=
ENST00000443358.6:c.492C>T	ENSP00000392451.2:p.Ser164=
ENST00000535067.5:c.358-2216C>T	ENSP00000443969.1:n.358-2216C>T
ENST00000537484.1:c.501C>T	ENSP00000440179.1:p.Ser167=
ENST00000542167.2:c.417C>T	ENSP00000438948.1:p.Ser139=
ENST00000543754.1:n.397C>T
NM_001002019.2:c.492C>T	NP_001002019.1:p.Ser164=
NM_001002020.2:c.492C>T	NP_001002020.1:p.Ser164=
NM_025215.5:c.576C>T	NP_079491.2:p.Ser192=
XM_011538768.1:c.177C>T	XP_011537070.1:p.Ser59=
XM_011538768.3:c.177C>T	XP_011537070.1:p.Ser59=
XR_001748872.1:n.1031C>T
NM_001002019.3:c.492C>T	NP_001002019.1:p.Ser164=
NM_001002020.3:c.492C>T	NP_001002020.1:p.Ser164=
NM_025215.6:c.576C>T MANE Select	NP_079491.2:p.Ser192=