Canonical Allele Identifier: CA373872013
Gene: PSAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304752A>T , CM000671.2:g.78304752A>T GRCh38
NC_000009.11:g.80919668A>T , CM000671.1:g.80919668A>T GRCh37
NC_000009.10:g.80109488A>T NCBI36
NG_012165.1:g.12610A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.209A>T MANE Select ENSP00000365773.3:p.Tyr70Phe
ENST00000347159.6:c.209A>T ENSP00000317606.2:p.Tyr70Phe
ENST00000376588.3:c.209A>T ENSP00000365773.3:p.Tyr70Phe
NM_021154.4:c.209A>T NP_066977.1:p.Tyr70Phe
NM_058179.3:c.209A>T NP_478059.1:p.Tyr70Phe
NM_058179.4:c.209A>T MANE Select NP_478059.1:p.Tyr70Phe
NM_021154.5:c.209A>T NP_066977.1:p.Tyr70Phe