Canonical Allele Identifier: CA1857665694

Gene: PSAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304751T= , CM000671.2:g.78304751T=	GRCh38
NC_000009.11:g.80919667T= , CM000671.1:g.80919667T=	GRCh37
NC_000009.10:g.80109487T=	NCBI36
NG_012165.1:g.12609T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.208T= MANE Select	ENSP00000365773.3:p.Tyr70=
ENST00000347159.6:c.208T=	ENSP00000317606.2:p.Tyr70=
ENST00000376588.3:c.208T=	ENSP00000365773.3:p.Tyr70=
NM_021154.4:c.208T=	NP_066977.1:p.Tyr70=
NM_058179.3:c.208T=	NP_478059.1:p.Tyr70=
NM_058179.4:c.208T= MANE Select	NP_478059.1:p.Tyr70=
NM_021154.5:c.208T=	NP_066977.1:p.Tyr70=