Canonical Allele Identifier: CA1857665689
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304736G= , CM000671.2:g.78304736G= GRCh38
NC_000009.11:g.80919652G= , CM000671.1:g.80919652G= GRCh37
NC_000009.10:g.80109472G= NCBI36
NG_012165.1:g.12594G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.193G= MANE Select ENSP00000365773.3:p.Ala65=
ENST00000347159.6:c.193G= ENSP00000317606.2:p.Ala65=
ENST00000376588.3:c.193G= ENSP00000365773.3:p.Ala65=
NM_021154.4:c.193G= NP_066977.1:p.Ala65=
NM_058179.3:c.193G= NP_478059.1:p.Ala65=
NM_058179.4:c.193G= MANE Select NP_478059.1:p.Ala65=
NM_021154.5:c.193G= NP_066977.1:p.Ala65=