Canonical Allele Identifier: CA2842873052
Gene: PSAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78300621dup , CM000671.2:g.78300621dup GRCh38
NC_000009.11:g.80915537dup , CM000671.1:g.80915537dup GRCh37
NC_000009.10:g.80105357dup NCBI36
NG_012165.1:g.8479dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.80dup MANE Select ENSP00000365773.3:p.Glu28GlyfsTer11
ENST00000347159.6:c.80dup ENSP00000317606.2:p.Glu28GlyfsTer11
ENST00000376588.3:c.80dup ENSP00000365773.3:p.Glu28GlyfsTer11
NM_021154.4:c.80dup NP_066977.1:p.Glu28GlyfsTer11
NM_058179.3:c.80dup NP_478059.1:p.Glu28GlyfsTer11
NM_058179.4:c.80dup MANE Select NP_478059.1:p.Glu28GlyfsTer11
NM_021154.5:c.80dup NP_066977.1:p.Glu28GlyfsTer11
Search 100 bp 5'
Search 100 bp 3'