Canonical Allele Identifier: CA1857665750

Gene: PSAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304900G= , CM000671.2:g.78304900G=	GRCh38
NC_000009.11:g.80919816G= , CM000671.1:g.80919816G=	GRCh37
NC_000009.10:g.80109636G=	NCBI36
NG_012165.1:g.12758G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.357G= MANE Select	ENSP00000365773.3:p.Gly119=
ENST00000347159.6:c.357G=	ENSP00000317606.2:p.Gly119=
ENST00000376588.3:c.357G=	ENSP00000365773.3:p.Gly119=
NM_021154.4:c.357G=	NP_066977.1:p.Gly119=
NM_058179.3:c.357G=	NP_478059.1:p.Gly119=
NM_058179.4:c.357G= MANE Select	NP_478059.1:p.Gly119=
NM_021154.5:c.357G=	NP_066977.1:p.Gly119=