Canonical Allele Identifier: CA1857677108

Gene: PSAT1

Linked Data

• dbSNP Id: rs1828556358

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78329987T>C , CM000671.2:g.78329987T>C	GRCh38
NC_000009.11:g.80944903T>C , CM000671.1:g.80944903T>C	GRCh37
NC_000009.10:g.80134723T>C	NCBI36
NG_012165.1:g.37845T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376588.4:c.*901T>C MANE Select	ENSP00000365773.3:n.*901T>C
ENST00000376588.3:c.*901T>C	ENSP00000365773.3:n.*901T>C
NM_021154.4:c.*901T>C	NP_066977.1:n.*901T>C
NM_058179.3:c.*901T>C	NP_478059.1:n.*901T>C
NM_058179.4:c.*901T>C MANE Select	NP_478059.1:n.*901T>C
NM_021154.5:c.*901T>C	NP_066977.1:n.*901T>C