Canonical Allele Identifier: CA373872373
Gene: PSAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304860C>G , CM000671.2:g.78304860C>G GRCh38
NC_000009.11:g.80919776C>G , CM000671.1:g.80919776C>G GRCh37
NC_000009.10:g.80109596C>G NCBI36
NG_012165.1:g.12718C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.317C>G MANE Select ENSP00000365773.3:p.Ala106Gly
ENST00000347159.6:c.317C>G ENSP00000317606.2:p.Ala106Gly
ENST00000376588.3:c.317C>G ENSP00000365773.3:p.Ala106Gly
NM_021154.4:c.317C>G NP_066977.1:p.Ala106Gly
NM_058179.3:c.317C>G NP_478059.1:p.Ala106Gly
NM_058179.4:c.317C>G MANE Select NP_478059.1:p.Ala106Gly
NM_021154.5:c.317C>G NP_066977.1:p.Ala106Gly