Canonical Allele Identifier: CA1857677066
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329872T= , CM000671.2:g.78329872T= GRCh38
NC_000009.11:g.80944788T= , CM000671.1:g.80944788T= GRCh37
NC_000009.10:g.80134608T= NCBI36
NG_012165.1:g.37730T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*786T= MANE Select ENSP00000365773.3:n.*786T=
ENST00000376588.3:c.*786T= ENSP00000365773.3:n.*786T=
NM_021154.4:c.*786T= NP_066977.1:n.*786T=
NM_058179.3:c.*786T= NP_478059.1:n.*786T=
NM_058179.4:c.*786T= MANE Select NP_478059.1:n.*786T=
NM_021154.5:c.*786T= NP_066977.1:n.*786T=