Canonical Allele Identifier: CA482842196

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132426063C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941518C>G , CM000674.2:g.131941518C>G	GRCh38
NC_000012.11:g.132426063C>G , CM000674.1:g.132426063C>G	GRCh37
NC_000012.10:g.130992016C>G	NCBI36
NG_013039.1:g.17319C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.771C>G MANE Select	ENSP00000365837.3:p.Pro257=
ENST00000322060.9:c.687C>G	ENSP00000324726.5:p.Pro229=
ENST00000376649.7:c.771C>G	ENSP00000365837.3:p.Pro257=
ENST00000443358.6:c.687C>G	ENSP00000392451.2:p.Pro229=
ENST00000535067.5:c.358-2021C>G	ENSP00000443969.1:n.358-2021C>G
ENST00000542167.2:c.612C>G	ENSP00000438948.1:p.Pro204=
ENST00000543754.1:n.592C>G
NM_001002019.2:c.687C>G	NP_001002019.1:p.Pro229=
NM_001002020.2:c.687C>G	NP_001002020.1:p.Pro229=
NM_025215.5:c.771C>G	NP_079491.2:p.Pro257=
XM_011538768.1:c.372C>G	XP_011537070.1:p.Pro124=
XM_011538768.3:c.372C>G	XP_011537070.1:p.Pro124=
XR_001748872.1:n.1226C>G
NM_001002019.3:c.687C>G	NP_001002019.1:p.Pro229=
NM_001002020.3:c.687C>G	NP_001002020.1:p.Pro229=
NM_025215.6:c.771C>G MANE Select	NP_079491.2:p.Pro257=