Canonical Allele Identifier: CA2542983245
Gene: PSAT1 HGNC NCBI

Linked Data

gnomAD v4: 9-78329843-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329843G>C , CM000671.2:g.78329843G>C GRCh38
NC_000009.11:g.80944759G>C , CM000671.1:g.80944759G>C GRCh37
NC_000009.10:g.80134579G>C NCBI36
NG_012165.1:g.37701G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*757G>C MANE Select ENSP00000365773.3:n.*757G>C
ENST00000376588.3:c.*757G>C ENSP00000365773.3:n.*757G>C
NM_021154.4:c.*757G>C NP_066977.1:n.*757G>C
NM_058179.3:c.*757G>C NP_478059.1:n.*757G>C
NM_058179.4:c.*757G>C MANE Select NP_478059.1:n.*757G>C
NM_021154.5:c.*757G>C NP_066977.1:n.*757G>C