Canonical Allele Identifier: CA1857665729

Gene: PSAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304842A= , CM000671.2:g.78304842A=	GRCh38
NC_000009.11:g.80919758A= , CM000671.1:g.80919758A=	GRCh37
NC_000009.10:g.80109578A=	NCBI36
NG_012165.1:g.12700A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.299A= MANE Select	ENSP00000365773.3:p.Asp100=
ENST00000347159.6:c.299A=	ENSP00000317606.2:p.Asp100=
ENST00000376588.3:c.299A=	ENSP00000365773.3:p.Asp100=
NM_021154.4:c.299A=	NP_066977.1:p.Asp100=
NM_058179.3:c.299A=	NP_478059.1:p.Asp100=
NM_058179.4:c.299A= MANE Select	NP_478059.1:p.Asp100=
NM_021154.5:c.299A=	NP_066977.1:p.Asp100=