Canonical Allele Identifier: CA482842189

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132426054G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941509G>T , CM000674.2:g.131941509G>T	GRCh38
NC_000012.11:g.132426054G>T , CM000674.1:g.132426054G>T	GRCh37
NC_000012.10:g.130992007G>T	NCBI36
NG_013039.1:g.17310G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.762G>T MANE Select	ENSP00000365837.3:p.Pro254=
ENST00000322060.9:c.678G>T	ENSP00000324726.5:p.Pro226=
ENST00000376649.7:c.762G>T	ENSP00000365837.3:p.Pro254=
ENST00000443358.6:c.678G>T	ENSP00000392451.2:p.Pro226=
ENST00000535067.5:c.358-2030G>T	ENSP00000443969.1:n.358-2030G>T
ENST00000542167.2:c.603G>T	ENSP00000438948.1:p.Pro201=
ENST00000543754.1:n.583G>T
NM_001002019.2:c.678G>T	NP_001002019.1:p.Pro226=
NM_001002020.2:c.678G>T	NP_001002020.1:p.Pro226=
NM_025215.5:c.762G>T	NP_079491.2:p.Pro254=
XM_011538768.1:c.363G>T	XP_011537070.1:p.Pro121=
XM_011538768.3:c.363G>T	XP_011537070.1:p.Pro121=
XR_001748872.1:n.1217G>T
NM_001002019.3:c.678G>T	NP_001002019.1:p.Pro226=
NM_001002020.3:c.678G>T	NP_001002020.1:p.Pro226=
NM_025215.6:c.762G>T MANE Select	NP_079491.2:p.Pro254=