Canonical Allele Identifier: CA373872509
Gene: PSAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304902C>A , CM000671.2:g.78304902C>A GRCh38
NC_000009.11:g.80919818C>A , CM000671.1:g.80919818C>A GRCh37
NC_000009.10:g.80109638C>A NCBI36
NG_012165.1:g.12760C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.359C>A MANE Select ENSP00000365773.3:p.Thr120Asn
ENST00000347159.6:c.359C>A ENSP00000317606.2:p.Thr120Asn
ENST00000376588.3:c.359C>A ENSP00000365773.3:p.Thr120Asn
NM_021154.4:c.359C>A NP_066977.1:p.Thr120Asn
NM_058179.3:c.359C>A NP_478059.1:p.Thr120Asn
NM_058179.4:c.359C>A MANE Select NP_478059.1:p.Thr120Asn
NM_021154.5:c.359C>A NP_066977.1:p.Thr120Asn