Canonical Allele Identifier: CA373872530
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80919828C>G (hg19) chr9:g.78304912C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304912C>G , CM000671.2:g.78304912C>G GRCh38
NC_000009.11:g.80919828C>G , CM000671.1:g.80919828C>G GRCh37
NC_000009.10:g.80109648C>G NCBI36
NG_012165.1:g.12770C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.369C>G MANE Select ENSP00000365773.3:p.Ile123Met
ENST00000347159.6:c.369C>G ENSP00000317606.2:p.Ile123Met
ENST00000376588.3:c.369C>G ENSP00000365773.3:p.Ile123Met
NM_021154.4:c.369C>G NP_066977.1:p.Ile123Met
NM_058179.3:c.369C>G NP_478059.1:p.Ile123Met
NM_058179.4:c.369C>G MANE Select NP_478059.1:p.Ile123Met
NM_021154.5:c.369C>G NP_066977.1:p.Ile123Met
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