Canonical Allele Identifier: CA1857665787
Gene: PSAT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304993C= , CM000671.2:g.78304993C= GRCh38
NC_000009.11:g.80919909C= , CM000671.1:g.80919909C= GRCh37
NC_000009.10:g.80109729C= NCBI36
NG_012165.1:g.12851C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.397+53C= MANE Select ENSP00000365773.3:n.397+53C=
ENST00000347159.6:c.397+53C= ENSP00000317606.2:n.397+53C=
ENST00000376588.3:c.397+53C= ENSP00000365773.3:n.397+53C=
NM_021154.4:c.397+53C= NP_066977.1:n.397+53C=
NM_058179.3:c.397+53C= NP_478059.1:n.397+53C=
NM_058179.4:c.397+53C= MANE Select NP_478059.1:n.397+53C=
NM_021154.5:c.397+53C= NP_066977.1:n.397+53C=
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