Canonical Allele Identifier: CA387298932

Gene: PUS1

Linked Data

• MyVariant Identifiers: chr12:g.132425963T>G (hg19) ; chr12:g.131941418T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941418T>G , CM000674.2:g.131941418T>G	GRCh38
NC_000012.11:g.132425963T>G , CM000674.1:g.132425963T>G	GRCh37
NC_000012.10:g.130991916T>G	NCBI36
NG_013039.1:g.17219T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376649.8:c.671T>G MANE Select	ENSP00000365837.3:p.Leu224Arg
ENST00000322060.9:c.587T>G	ENSP00000324726.5:p.Leu196Arg
ENST00000376649.7:c.671T>G	ENSP00000365837.3:p.Leu224Arg
ENST00000443358.6:c.587T>G	ENSP00000392451.2:p.Leu196Arg
ENST00000535067.5:c.358-2121T>G	ENSP00000443969.1:n.358-2121T>G
ENST00000537484.1:c.596T>G	ENSP00000440179.1:p.Leu199Arg
ENST00000542167.2:c.512T>G	ENSP00000438948.1:p.Leu171Arg
ENST00000543754.1:n.492T>G
NM_001002019.2:c.587T>G	NP_001002019.1:p.Leu196Arg
NM_001002020.2:c.587T>G	NP_001002020.1:p.Leu196Arg
NM_025215.5:c.671T>G	NP_079491.2:p.Leu224Arg
XM_011538768.1:c.272T>G	XP_011537070.1:p.Leu91Arg
XM_011538768.3:c.272T>G	XP_011537070.1:p.Leu91Arg
XR_001748872.1:n.1126T>G
NM_001002019.3:c.587T>G	NP_001002019.1:p.Leu196Arg
NM_001002020.3:c.587T>G	NP_001002020.1:p.Leu196Arg
NM_025215.6:c.671T>G MANE Select	NP_079491.2:p.Leu224Arg