Canonical Allele Identifier: CA6884310

Gene: PUS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131941815G>A , CM000674.2:g.131941815G>A	GRCh38
NC_000012.11:g.132426360G>A , CM000674.1:g.132426360G>A	GRCh37
NC_000012.10:g.130992313G>A	NCBI36
NG_013039.1:g.17616G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025215.6:c.1068G>A MANE Select	NP_079491.2:p.Leu356=
ENST00000376649.8:c.1068G>A MANE Select	ENSP00000365837.3:p.Leu356=
NM_001002019.2:c.984G>A	NP_001002019.1:p.Leu328=
NM_001002019.3:c.984G>A	NP_001002019.1:p.Leu328=
NM_001002020.2:c.984G>A	NP_001002020.1:p.Leu328=
NM_001002020.3:c.984G>A	NP_001002020.1:p.Leu328=
NM_025215.5:c.1068G>A	NP_079491.2:p.Leu356=
ENST00000322060.9:c.984G>A	ENSP00000324726.5:p.Leu328=
ENST00000376649.7:c.1068G>A	ENSP00000365837.3:p.Leu356=
ENST00000443358.6:c.984G>A	ENSP00000392451.2:p.Leu328=
ENST00000535067.5:c.358-1724G>A	ENSP00000443969.1:n.358-1724G>A
ENST00000542167.2:c.909G>A	ENSP00000438948.1:p.Leu303=
ENST00000543754.1:n.889G>A
XM_011538768.1:c.669G>A	XP_011537070.1:p.Leu223=
XM_011538768.3:c.669G>A	XP_011537070.1:p.Leu223=
XR_001748872.1:n.1523G>A