Canonical Allele Identifier: CA2072621136

Gene: PUS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941464C= , CM000674.2:g.131941464C=	GRCh38
NC_000012.11:g.132426009C= , CM000674.1:g.132426009C=	GRCh37
NC_000012.10:g.130991962C=	NCBI36
NG_013039.1:g.17265C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.717C= MANE Select	ENSP00000365837.3:p.Tyr239=
ENST00000322060.9:c.633C=	ENSP00000324726.5:p.Tyr211=
ENST00000376649.7:c.717C=	ENSP00000365837.3:p.Tyr239=
ENST00000443358.6:c.633C=	ENSP00000392451.2:p.Tyr211=
ENST00000535067.5:c.358-2075C=	ENSP00000443969.1:n.358-2075C=
ENST00000542167.2:c.558C=	ENSP00000438948.1:p.Tyr186=
ENST00000543754.1:n.538C=
NM_001002019.2:c.633C=	NP_001002019.1:p.Tyr211=
NM_001002020.2:c.633C=	NP_001002020.1:p.Tyr211=
NM_025215.5:c.717C=	NP_079491.2:p.Tyr239=
XM_011538768.1:c.318C=	XP_011537070.1:p.Tyr106=
XM_011538768.3:c.318C=	XP_011537070.1:p.Tyr106=
XR_001748872.1:n.1172C=
NM_001002019.3:c.633C=	NP_001002019.1:p.Tyr211=
NM_001002020.3:c.633C=	NP_001002020.1:p.Tyr211=
NM_025215.6:c.717C= MANE Select	NP_079491.2:p.Tyr239=