Canonical Allele Identifier: CA1857677103
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329979G= , CM000671.2:g.78329979G= GRCh38
NC_000009.11:g.80944895G= , CM000671.1:g.80944895G= GRCh37
NC_000009.10:g.80134715G= NCBI36
NG_012165.1:g.37837G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*893G= MANE Select ENSP00000365773.3:n.*893G=
ENST00000376588.3:c.*893G= ENSP00000365773.3:n.*893G=
NM_021154.4:c.*893G= NP_066977.1:n.*893G=
NM_058179.3:c.*893G= NP_478059.1:n.*893G=
NM_058179.4:c.*893G= MANE Select NP_478059.1:n.*893G=
NM_021154.5:c.*893G= NP_066977.1:n.*893G=