Canonical Allele Identifier: CA1857665727
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304839C= , CM000671.2:g.78304839C= GRCh38
NC_000009.11:g.80919755C= , CM000671.1:g.80919755C= GRCh37
NC_000009.10:g.80109575C= NCBI36
NG_012165.1:g.12697C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.296C= MANE Select ENSP00000365773.3:p.Ala99=
ENST00000347159.6:c.296C= ENSP00000317606.2:p.Ala99=
ENST00000376588.3:c.296C= ENSP00000365773.3:p.Ala99=
NM_021154.4:c.296C= NP_066977.1:p.Ala99=
NM_058179.3:c.296C= NP_478059.1:p.Ala99=
NM_058179.4:c.296C= MANE Select NP_478059.1:p.Ala99=
NM_021154.5:c.296C= NP_066977.1:p.Ala99=