Canonical Allele Identifier: CA1857665783
Gene: PSAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304984G= , CM000671.2:g.78304984G= GRCh38
NC_000009.11:g.80919900G= , CM000671.1:g.80919900G= GRCh37
NC_000009.10:g.80109720G= NCBI36
NG_012165.1:g.12842G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.397+44G= MANE Select ENSP00000365773.3:n.397+44G=
ENST00000347159.6:c.397+44G= ENSP00000317606.2:n.397+44G=
ENST00000376588.3:c.397+44G= ENSP00000365773.3:n.397+44G=
NM_021154.4:c.397+44G= NP_066977.1:n.397+44G=
NM_058179.3:c.397+44G= NP_478059.1:n.397+44G=
NM_058179.4:c.397+44G= MANE Select NP_478059.1:n.397+44G=
NM_021154.5:c.397+44G= NP_066977.1:n.397+44G=
Search 100 bp 5'
Search 100 bp 3'