Canonical Allele Identifier: CA482841954

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132425943T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941398T>A , CM000674.2:g.131941398T>A	GRCh38
NC_000012.11:g.132425943T>A , CM000674.1:g.132425943T>A	GRCh37
NC_000012.10:g.130991896T>A	NCBI36
NG_013039.1:g.17199T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.651T>A MANE Select	ENSP00000365837.3:p.Val217=
ENST00000322060.9:c.567T>A	ENSP00000324726.5:p.Val189=
ENST00000376649.7:c.651T>A	ENSP00000365837.3:p.Val217=
ENST00000443358.6:c.567T>A	ENSP00000392451.2:p.Val189=
ENST00000535067.5:c.358-2141T>A	ENSP00000443969.1:n.358-2141T>A
ENST00000537484.1:c.576T>A	ENSP00000440179.1:p.Val192=
ENST00000542167.2:c.492T>A	ENSP00000438948.1:p.Val164=
ENST00000543754.1:n.472T>A
NM_001002019.2:c.567T>A	NP_001002019.1:p.Val189=
NM_001002020.2:c.567T>A	NP_001002020.1:p.Val189=
NM_025215.5:c.651T>A	NP_079491.2:p.Val217=
XM_011538768.1:c.252T>A	XP_011537070.1:p.Val84=
XM_011538768.3:c.252T>A	XP_011537070.1:p.Val84=
XR_001748872.1:n.1106T>A
NM_001002019.3:c.567T>A	NP_001002019.1:p.Val189=
NM_001002020.3:c.567T>A	NP_001002020.1:p.Val189=
NM_025215.6:c.651T>A MANE Select	NP_079491.2:p.Val217=