Canonical Allele Identifier: CA373872540
Gene: PSAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304917A>T , CM000671.2:g.78304917A>T GRCh38
NC_000009.11:g.80919833A>T , CM000671.1:g.80919833A>T GRCh37
NC_000009.10:g.80109653A>T NCBI36
NG_012165.1:g.12775A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.374A>T MANE Select ENSP00000365773.3:p.His125Leu
ENST00000347159.6:c.374A>T ENSP00000317606.2:p.His125Leu
ENST00000376588.3:c.374A>T ENSP00000365773.3:p.His125Leu
NM_021154.4:c.374A>T NP_066977.1:p.His125Leu
NM_058179.3:c.374A>T NP_478059.1:p.His125Leu
NM_058179.4:c.374A>T MANE Select NP_478059.1:p.His125Leu
NM_021154.5:c.374A>T NP_066977.1:p.His125Leu