Canonical Allele Identifier: CA373871974

Gene: PSAT1

Linked Data

• MyVariant Identifiers: chr9:g.80919649A>T (hg19) ; chr9:g.78304733A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304733A>T , CM000671.2:g.78304733A>T	GRCh38
NC_000009.11:g.80919649A>T , CM000671.1:g.80919649A>T	GRCh37
NC_000009.10:g.80109469A>T	NCBI36
NG_012165.1:g.12591A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.192-2A>T MANE Select	ENSP00000365773.3:n.192-2A>T
ENST00000347159.6:c.192-2A>T	ENSP00000317606.2:n.192-2A>T
ENST00000376588.3:c.192-2A>T	ENSP00000365773.3:n.192-2A>T
NM_021154.4:c.192-2A>T	NP_066977.1:n.192-2A>T
NM_058179.3:c.192-2A>T	NP_478059.1:n.192-2A>T
NM_058179.4:c.192-2A>T MANE Select	NP_478059.1:n.192-2A>T
NM_021154.5:c.192-2A>T	NP_066977.1:n.192-2A>T