Canonical Allele Identifier: CA373872006
Gene: PSAT1 HGNC NCBI

Linked Data

gnomAD v4: 9-78304749-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304749A>G , CM000671.2:g.78304749A>G GRCh38
NC_000009.11:g.80919665A>G , CM000671.1:g.80919665A>G GRCh37
NC_000009.10:g.80109485A>G NCBI36
NG_012165.1:g.12607A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.206A>G MANE Select ENSP00000365773.3:p.Asn69Ser
ENST00000347159.6:c.206A>G ENSP00000317606.2:p.Asn69Ser
ENST00000376588.3:c.206A>G ENSP00000365773.3:p.Asn69Ser
NM_021154.4:c.206A>G NP_066977.1:p.Asn69Ser
NM_058179.3:c.206A>G NP_478059.1:p.Asn69Ser
NM_058179.4:c.206A>G MANE Select NP_478059.1:p.Asn69Ser
NM_021154.5:c.206A>G NP_066977.1:p.Asn69Ser