Canonical Allele Identifier: CA5095563
Gene: PSAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 976978
ClinVar RCV Id: RCV001254490
dbSNP Id: rs748059814
gnomAD v2: 9-80919662-A-G
gnomAD v4: 9-78304746-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304746A>G , CM000671.2:g.78304746A>G GRCh38
NC_000009.11:g.80919662A>G , CM000671.1:g.80919662A>G GRCh37
NC_000009.10:g.80109482A>G NCBI36
NG_012165.1:g.12604A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.203A>G MANE Select ENSP00000365773.3:p.Asp68Gly
ENST00000347159.6:c.203A>G ENSP00000317606.2:p.Asp68Gly
ENST00000376588.3:c.203A>G ENSP00000365773.3:p.Asp68Gly
NM_021154.4:c.203A>G NP_066977.1:p.Asp68Gly
NM_058179.3:c.203A>G NP_478059.1:p.Asp68Gly
NM_058179.4:c.203A>G MANE Select NP_478059.1:p.Asp68Gly
NM_021154.5:c.203A>G NP_066977.1:p.Asp68Gly