Canonical Allele Identifier: CA867185057

Gene: PSAT1

Linked Data

• dbSNP Id: rs1452301969
• gnomAD v3: 9-78304715-T-C
• gnomAD v4: 9-78304715-T-C
• MyVariant Identifiers: chr9:g.80919631T>C (hg19) ; chr9:g.78304715T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78304715T>C , CM000671.2:g.78304715T>C	GRCh38
NC_000009.11:g.80919631T>C , CM000671.1:g.80919631T>C	GRCh37
NC_000009.10:g.80109451T>C	NCBI36
NG_012165.1:g.12573T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376588.4:c.192-20T>C MANE Select	ENSP00000365773.3:n.192-20T>C
ENST00000347159.6:c.192-20T>C	ENSP00000317606.2:n.192-20T>C
ENST00000376588.3:c.192-20T>C	ENSP00000365773.3:n.192-20T>C
NM_021154.4:c.192-20T>C	NP_066977.1:n.192-20T>C
NM_058179.3:c.192-20T>C	NP_478059.1:n.192-20T>C
NM_058179.4:c.192-20T>C MANE Select	NP_478059.1:n.192-20T>C
NM_021154.5:c.192-20T>C	NP_066977.1:n.192-20T>C