Canonical Allele Identifier: CA465542749
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80915568T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78300652T>A , CM000671.2:g.78300652T>A GRCh38
NC_000009.11:g.80915568T>A , CM000671.1:g.80915568T>A GRCh37
NC_000009.10:g.80105388T>A NCBI36
NG_012165.1:g.8510T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.111T>A MANE Select ENSP00000365773.3:p.Ile37=
ENST00000347159.6:c.111T>A ENSP00000317606.2:p.Ile37=
ENST00000376588.3:c.111T>A ENSP00000365773.3:p.Ile37=
NM_021154.4:c.111T>A NP_066977.1:p.Ile37=
NM_058179.3:c.111T>A NP_478059.1:p.Ile37=
NM_058179.4:c.111T>A MANE Select NP_478059.1:p.Ile37=
NM_021154.5:c.111T>A NP_066977.1:p.Ile37=
Search 100 bp 5'
Search 100 bp 3'