Canonical Allele Identifier: CA1857677060
Gene: PSAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1828554867
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329851T>G , CM000671.2:g.78329851T>G GRCh38
NC_000009.11:g.80944767T>G , CM000671.1:g.80944767T>G GRCh37
NC_000009.10:g.80134587T>G NCBI36
NG_012165.1:g.37709T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*765T>G MANE Select ENSP00000365773.3:n.*765T>G
ENST00000376588.3:c.*765T>G ENSP00000365773.3:n.*765T>G
NM_021154.4:c.*765T>G NP_066977.1:n.*765T>G
NM_058179.3:c.*765T>G NP_478059.1:n.*765T>G
NM_058179.4:c.*765T>G MANE Select NP_478059.1:n.*765T>G
NM_021154.5:c.*765T>G NP_066977.1:n.*765T>G
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