Canonical Allele Identifier: CA465542998
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80919822A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304906A>C , CM000671.2:g.78304906A>C GRCh38
NC_000009.11:g.80919822A>C , CM000671.1:g.80919822A>C GRCh37
NC_000009.10:g.80109642A>C NCBI36
NG_012165.1:g.12764A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.363A>C MANE Select ENSP00000365773.3:p.Ile121=
ENST00000347159.6:c.363A>C ENSP00000317606.2:p.Ile121=
ENST00000376588.3:c.363A>C ENSP00000365773.3:p.Ile121=
NM_021154.4:c.363A>C NP_066977.1:p.Ile121=
NM_058179.3:c.363A>C NP_478059.1:p.Ile121=
NM_058179.4:c.363A>C MANE Select NP_478059.1:p.Ile121=
NM_021154.5:c.363A>C NP_066977.1:p.Ile121=
Search 100 bp 5'
Search 100 bp 3'