Canonical Allele Identifier: CA1857677054
Gene: PSAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329822_78329823delinsCT , CM000671.2:g.78329822_78329823delinsCT GRCh38
NC_000009.11:g.80944738_80944739delinsCT , CM000671.1:g.80944738_80944739delinsCT GRCh37
NC_000009.10:g.80134558_80134559delinsCT NCBI36
NG_012165.1:g.37680_37681delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*736_*737delinsCT MANE Select ENSP00000365773.3:n.*736_*737delinsCT
ENST00000376588.3:c.*736_*737delinsCT ENSP00000365773.3:n.*736_*737delinsCT
NM_021154.4:c.*736_*737delinsCT NP_066977.1:n.*736_*737delinsCT
NM_058179.3:c.*736_*737delinsCT NP_478059.1:n.*736_*737delinsCT
NM_058179.4:c.*736_*737delinsCT MANE Select NP_478059.1:n.*736_*737delinsCT
NM_021154.5:c.*736_*737delinsCT NP_066977.1:n.*736_*737delinsCT
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