Canonical Allele Identifier: CA194419392
Gene: PSAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1007957619
MyVariant Identifiers: chr9:g.80944788T>A (hg19) chr9:g.78329872T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329872T>A , CM000671.2:g.78329872T>A GRCh38
NC_000009.11:g.80944788T>A , CM000671.1:g.80944788T>A GRCh37
NC_000009.10:g.80134608T>A NCBI36
NG_012165.1:g.37730T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*786T>A MANE Select ENSP00000365773.3:n.*786T>A
ENST00000376588.3:c.*786T>A ENSP00000365773.3:n.*786T>A
NM_021154.4:c.*786T>A NP_066977.1:n.*786T>A
NM_058179.3:c.*786T>A NP_478059.1:n.*786T>A
NM_058179.4:c.*786T>A MANE Select NP_478059.1:n.*786T>A
NM_021154.5:c.*786T>A NP_066977.1:n.*786T>A
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