Canonical Allele Identifier: CA5095565
Gene: PSAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 976982
ClinVar RCV Id: RCV001254494
dbSNP Id: rs542332287
gnomAD v2: 9-80919672-G-T
gnomAD v3: 9-78304756-G-T
gnomAD v4: 9-78304756-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304756G>T , CM000671.2:g.78304756G>T GRCh38
NC_000009.11:g.80919672G>T , CM000671.1:g.80919672G>T GRCh37
NC_000009.10:g.80109492G>T NCBI36
NG_012165.1:g.12614G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376588.4:c.213G>T MANE Select ENSP00000365773.3:p.Lys71Asn
ENST00000347159.6:c.213G>T ENSP00000317606.2:p.Lys71Asn
ENST00000376588.3:c.213G>T ENSP00000365773.3:p.Lys71Asn
NM_021154.4:c.213G>T NP_066977.1:p.Lys71Asn
NM_058179.3:c.213G>T NP_478059.1:p.Lys71Asn
NM_058179.4:c.213G>T MANE Select NP_478059.1:p.Lys71Asn
NM_021154.5:c.213G>T NP_066977.1:p.Lys71Asn