Canonical Allele Identifier: CA465542751
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80915571T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78300655T>C , CM000671.2:g.78300655T>C GRCh38
NC_000009.11:g.80915571T>C , CM000671.1:g.80915571T>C GRCh37
NC_000009.10:g.80105391T>C NCBI36
NG_012165.1:g.8513T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.114T>C MANE Select ENSP00000365773.3:p.Ser38=
ENST00000347159.6:c.114T>C ENSP00000317606.2:p.Ser38=
ENST00000376588.3:c.114T>C ENSP00000365773.3:p.Ser38=
NM_021154.4:c.114T>C NP_066977.1:p.Ser38=
NM_058179.3:c.114T>C NP_478059.1:p.Ser38=
NM_058179.4:c.114T>C MANE Select NP_478059.1:p.Ser38=
NM_021154.5:c.114T>C NP_066977.1:p.Ser38=
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