Canonical Allele Identifier: CA482842002

Gene: PUS1

Linked Data

• dbSNP Id: rs1891059596
• MyVariant Identifiers: chr12:g.132425970C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941425C>G , CM000674.2:g.131941425C>G	GRCh38
NC_000012.11:g.132425970C>G , CM000674.1:g.132425970C>G	GRCh37
NC_000012.10:g.130991923C>G	NCBI36
NG_013039.1:g.17226C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.678C>G MANE Select	ENSP00000365837.3:p.Ala226=
ENST00000322060.9:c.594C>G	ENSP00000324726.5:p.Ala198=
ENST00000376649.7:c.678C>G	ENSP00000365837.3:p.Ala226=
ENST00000443358.6:c.594C>G	ENSP00000392451.2:p.Ala198=
ENST00000535067.5:c.358-2114C>G	ENSP00000443969.1:n.358-2114C>G
ENST00000542167.2:c.519C>G	ENSP00000438948.1:p.Ala173=
ENST00000543754.1:n.499C>G
NM_001002019.2:c.594C>G	NP_001002019.1:p.Ala198=
NM_001002020.2:c.594C>G	NP_001002020.1:p.Ala198=
NM_025215.5:c.678C>G	NP_079491.2:p.Ala226=
XM_011538768.1:c.279C>G	XP_011537070.1:p.Ala93=
XM_011538768.3:c.279C>G	XP_011537070.1:p.Ala93=
XR_001748872.1:n.1133C>G
NM_001002019.3:c.594C>G	NP_001002019.1:p.Ala198=
NM_001002020.3:c.594C>G	NP_001002020.1:p.Ala198=
NM_025215.6:c.678C>G MANE Select	NP_079491.2:p.Ala226=