Canonical Allele Identifier: CA465542997

Gene: PSAT1

Linked Data

• MyVariant Identifiers: chr9:g.80919822A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304906A>T , CM000671.2:g.78304906A>T	GRCh38
NC_000009.11:g.80919822A>T , CM000671.1:g.80919822A>T	GRCh37
NC_000009.10:g.80109642A>T	NCBI36
NG_012165.1:g.12764A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.363A>T MANE Select	ENSP00000365773.3:p.Ile121=
ENST00000347159.6:c.363A>T	ENSP00000317606.2:p.Ile121=
ENST00000376588.3:c.363A>T	ENSP00000365773.3:p.Ile121=
NM_021154.4:c.363A>T	NP_066977.1:p.Ile121=
NM_058179.3:c.363A>T	NP_478059.1:p.Ile121=
NM_058179.4:c.363A>T MANE Select	NP_478059.1:p.Ile121=
NM_021154.5:c.363A>T	NP_066977.1:p.Ile121=