Canonical Allele Identifier: CA1857665692
Gene: PSAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304743C= , CM000671.2:g.78304743C= GRCh38
NC_000009.11:g.80919659C= , CM000671.1:g.80919659C= GRCh37
NC_000009.10:g.80109479C= NCBI36
NG_012165.1:g.12601C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.200C= MANE Select ENSP00000365773.3:p.Pro67=
ENST00000347159.6:c.200C= ENSP00000317606.2:p.Pro67=
ENST00000376588.3:c.200C= ENSP00000365773.3:p.Pro67=
NM_021154.4:c.200C= NP_066977.1:p.Pro67=
NM_058179.3:c.200C= NP_478059.1:p.Pro67=
NM_058179.4:c.200C= MANE Select NP_478059.1:p.Pro67=
NM_021154.5:c.200C= NP_066977.1:p.Pro67=