Canonical Allele Identifier: CA1857665697
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304754A= , CM000671.2:g.78304754A= GRCh38
NC_000009.11:g.80919670A= , CM000671.1:g.80919670A= GRCh37
NC_000009.10:g.80109490A= NCBI36
NG_012165.1:g.12612A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.211A= MANE Select ENSP00000365773.3:p.Lys71=
ENST00000347159.6:c.211A= ENSP00000317606.2:p.Lys71=
ENST00000376588.3:c.211A= ENSP00000365773.3:p.Lys71=
NM_021154.4:c.211A= NP_066977.1:p.Lys71=
NM_058179.3:c.211A= NP_478059.1:p.Lys71=
NM_058179.4:c.211A= MANE Select NP_478059.1:p.Lys71=
NM_021154.5:c.211A= NP_066977.1:p.Lys71=