Canonical Allele Identifier: CA465542970
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80919777T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304861T>A , CM000671.2:g.78304861T>A GRCh38
NC_000009.11:g.80919777T>A , CM000671.1:g.80919777T>A GRCh37
NC_000009.10:g.80109597T>A NCBI36
NG_012165.1:g.12719T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.318T>A MANE Select ENSP00000365773.3:p.Ala106=
ENST00000347159.6:c.318T>A ENSP00000317606.2:p.Ala106=
ENST00000376588.3:c.318T>A ENSP00000365773.3:p.Ala106=
NM_021154.4:c.318T>A NP_066977.1:p.Ala106=
NM_058179.3:c.318T>A NP_478059.1:p.Ala106=
NM_058179.4:c.318T>A MANE Select NP_478059.1:p.Ala106=
NM_021154.5:c.318T>A NP_066977.1:p.Ala106=
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