Canonical Allele Identifier: CA482841661

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132425887A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941342A>C , CM000674.2:g.131941342A>C	GRCh38
NC_000012.11:g.132425887A>C , CM000674.1:g.132425887A>C	GRCh37
NC_000012.10:g.130991840A>C	NCBI36
NG_013039.1:g.17143A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.595A>C MANE Select	ENSP00000365837.3:p.Arg199=
ENST00000322060.9:c.511A>C	ENSP00000324726.5:p.Arg171=
ENST00000376649.7:c.595A>C	ENSP00000365837.3:p.Arg199=
ENST00000443358.6:c.511A>C	ENSP00000392451.2:p.Arg171=
ENST00000535067.5:c.358-2197A>C	ENSP00000443969.1:n.358-2197A>C
ENST00000537484.1:c.520A>C	ENSP00000440179.1:p.Arg174=
ENST00000542167.2:c.436A>C	ENSP00000438948.1:p.Arg146=
ENST00000543754.1:n.416A>C
NM_001002019.2:c.511A>C	NP_001002019.1:p.Arg171=
NM_001002020.2:c.511A>C	NP_001002020.1:p.Arg171=
NM_025215.5:c.595A>C	NP_079491.2:p.Arg199=
XM_011538768.1:c.196A>C	XP_011537070.1:p.Arg66=
XM_011538768.3:c.196A>C	XP_011537070.1:p.Arg66=
XR_001748872.1:n.1050A>C
NM_001002019.3:c.511A>C	NP_001002019.1:p.Arg171=
NM_001002020.3:c.511A>C	NP_001002020.1:p.Arg171=
NM_025215.6:c.595A>C MANE Select	NP_079491.2:p.Arg199=