Canonical Allele Identifier: CA1857663829

Gene: PSAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78300652T= , CM000671.2:g.78300652T=	GRCh38
NC_000009.11:g.80915568T= , CM000671.1:g.80915568T=	GRCh37
NC_000009.10:g.80105388T=	NCBI36
NG_012165.1:g.8510T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376588.4:c.111T= MANE Select	ENSP00000365773.3:p.Ile37=
ENST00000347159.6:c.111T=	ENSP00000317606.2:p.Ile37=
ENST00000376588.3:c.111T=	ENSP00000365773.3:p.Ile37=
NM_021154.4:c.111T=	NP_066977.1:p.Ile37=
NM_058179.3:c.111T=	NP_478059.1:p.Ile37=
NM_058179.4:c.111T= MANE Select	NP_478059.1:p.Ile37=
NM_021154.5:c.111T=	NP_066977.1:p.Ile37=