Canonical Allele Identifier: CA465542989

Gene: PSAT1

Linked Data

• MyVariant Identifiers: chr9:g.80919804C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304888C>G , CM000671.2:g.78304888C>G	GRCh38
NC_000009.11:g.80919804C>G , CM000671.1:g.80919804C>G	GRCh37
NC_000009.10:g.80109624C>G	NCBI36
NG_012165.1:g.12746C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.345C>G MANE Select	ENSP00000365773.3:p.Ala115=
ENST00000347159.6:c.345C>G	ENSP00000317606.2:p.Ala115=
ENST00000376588.3:c.345C>G	ENSP00000365773.3:p.Ala115=
NM_021154.4:c.345C>G	NP_066977.1:p.Ala115=
NM_058179.3:c.345C>G	NP_478059.1:p.Ala115=
NM_058179.4:c.345C>G MANE Select	NP_478059.1:p.Ala115=
NM_021154.5:c.345C>G	NP_066977.1:p.Ala115=