Canonical Allele Identifier: CA373871987
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80919656T>A (hg19) chr9:g.78304740T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304740T>A , CM000671.2:g.78304740T>A GRCh38
NC_000009.11:g.80919656T>A , CM000671.1:g.80919656T>A GRCh37
NC_000009.10:g.80109476T>A NCBI36
NG_012165.1:g.12598T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.197T>A MANE Select ENSP00000365773.3:p.Val66Asp
ENST00000347159.6:c.197T>A ENSP00000317606.2:p.Val66Asp
ENST00000376588.3:c.197T>A ENSP00000365773.3:p.Val66Asp
NM_021154.4:c.197T>A NP_066977.1:p.Val66Asp
NM_058179.3:c.197T>A NP_478059.1:p.Val66Asp
NM_058179.4:c.197T>A MANE Select NP_478059.1:p.Val66Asp
NM_021154.5:c.197T>A NP_066977.1:p.Val66Asp
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