Canonical Allele Identifier: CA1857677110
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329994G= , CM000671.2:g.78329994G= GRCh38
NC_000009.11:g.80944910G= , CM000671.1:g.80944910G= GRCh37
NC_000009.10:g.80134730G= NCBI36
NG_012165.1:g.37852G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*908G= MANE Select ENSP00000365773.3:n.*908G=
ENST00000376588.3:c.*908G= ENSP00000365773.3:n.*908G=
NM_021154.4:c.*908G= NP_066977.1:n.*908G=
NM_058179.3:c.*908G= NP_478059.1:n.*908G=
NM_058179.4:c.*908G= MANE Select NP_478059.1:n.*908G=
NM_021154.5:c.*908G= NP_066977.1:n.*908G=