Canonical Allele Identifier: CA867157026

Gene: PSAT1

Linked Data

• dbSNP Id: rs1326004618
• gnomAD v3: 9-78329890-A-G
• gnomAD v4: 9-78329890-A-G
• MyVariant Identifiers: chr9:g.80944806A>G (hg19) ; chr9:g.78329890A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78329890A>G , CM000671.2:g.78329890A>G	GRCh38
NC_000009.11:g.80944806A>G , CM000671.1:g.80944806A>G	GRCh37
NC_000009.10:g.80134626A>G	NCBI36
NG_012165.1:g.37748A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376588.4:c.*804A>G MANE Select	ENSP00000365773.3:n.*804A>G
ENST00000376588.3:c.*804A>G	ENSP00000365773.3:n.*804A>G
NM_021154.4:c.*804A>G	NP_066977.1:n.*804A>G
NM_058179.3:c.*804A>G	NP_478059.1:n.*804A>G
NM_058179.4:c.*804A>G MANE Select	NP_478059.1:n.*804A>G
NM_021154.5:c.*804A>G	NP_066977.1:n.*804A>G