Canonical Allele Identifier: CA2516523087
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329832A>G , CM000671.2:g.78329832A>G GRCh38
NC_000009.11:g.80944748A>G , CM000671.1:g.80944748A>G GRCh37
NC_000009.10:g.80134568A>G NCBI36
NG_012165.1:g.37690A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*746A>G MANE Select ENSP00000365773.3:n.*746A>G
ENST00000376588.3:c.*746A>G ENSP00000365773.3:n.*746A>G
NM_021154.4:c.*746A>G NP_066977.1:n.*746A>G
NM_058179.3:c.*746A>G NP_478059.1:n.*746A>G
NM_058179.4:c.*746A>G MANE Select NP_478059.1:n.*746A>G
NM_021154.5:c.*746A>G NP_066977.1:n.*746A>G