Canonical Allele Identifier: CA5095508

Gene: PSAT1

Linked Data

• dbSNP Id: rs752063667
• ExAC: 9:80915606 T / C
• gnomAD v2: 9-80915606-T-C
• gnomAD v4: 9-78300690-T-C
• MyVariant Identifiers: chr9:g.80915606T>C (hg19) ; chr9:g.78300690T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78300690T>C , CM000671.2:g.78300690T>C	GRCh38
NC_000009.11:g.80915606T>C , CM000671.1:g.80915606T>C	GRCh37
NC_000009.10:g.80105426T>C	NCBI36
NG_012165.1:g.8548T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.121+28T>C MANE Select	ENSP00000365773.3:n.121+28T>C
ENST00000347159.6:c.121+28T>C	ENSP00000317606.2:n.121+28T>C
ENST00000376588.3:c.121+28T>C	ENSP00000365773.3:n.121+28T>C
NM_021154.4:c.121+28T>C	NP_066977.1:n.121+28T>C
NM_058179.3:c.121+28T>C	NP_478059.1:n.121+28T>C
NM_058179.4:c.121+28T>C MANE Select	NP_478059.1:n.121+28T>C
NM_021154.5:c.121+28T>C	NP_066977.1:n.121+28T>C