Canonical Allele Identifier: CA1857677099
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329967A= , CM000671.2:g.78329967A= GRCh38
NC_000009.11:g.80944883A= , CM000671.1:g.80944883A= GRCh37
NC_000009.10:g.80134703A= NCBI36
NG_012165.1:g.37825A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*881A= MANE Select ENSP00000365773.3:n.*881A=
ENST00000376588.3:c.*881A= ENSP00000365773.3:n.*881A=
NM_021154.4:c.*881A= NP_066977.1:n.*881A=
NM_058179.3:c.*881A= NP_478059.1:n.*881A=
NM_058179.4:c.*881A= MANE Select NP_478059.1:n.*881A=
NM_021154.5:c.*881A= NP_066977.1:n.*881A=