Canonical Allele Identifier: CA373872557
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80919841C>A (hg19) chr9:g.78304925C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304925C>A , CM000671.2:g.78304925C>A GRCh38
NC_000009.11:g.80919841C>A , CM000671.1:g.80919841C>A GRCh37
NC_000009.10:g.80109661C>A NCBI36
NG_012165.1:g.12783C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.382C>A MANE Select ENSP00000365773.3:p.Leu128Ile
ENST00000347159.6:c.382C>A ENSP00000317606.2:p.Leu128Ile
ENST00000376588.3:c.382C>A ENSP00000365773.3:p.Leu128Ile
NM_021154.4:c.382C>A NP_066977.1:p.Leu128Ile
NM_058179.3:c.382C>A NP_478059.1:p.Leu128Ile
NM_058179.4:c.382C>A MANE Select NP_478059.1:p.Leu128Ile
NM_021154.5:c.382C>A NP_066977.1:p.Leu128Ile
Search 100 bp 5'
Search 100 bp 3'