Canonical Allele Identifier: CA373872014
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80919669T>A (hg19) chr9:g.78304753T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304753T>A , CM000671.2:g.78304753T>A GRCh38
NC_000009.11:g.80919669T>A , CM000671.1:g.80919669T>A GRCh37
NC_000009.10:g.80109489T>A NCBI36
NG_012165.1:g.12611T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.210T>A MANE Select ENSP00000365773.3:p.Tyr70Ter
ENST00000347159.6:c.210T>A ENSP00000317606.2:p.Tyr70Ter
ENST00000376588.3:c.210T>A ENSP00000365773.3:p.Tyr70Ter
NM_021154.4:c.210T>A NP_066977.1:p.Tyr70Ter
NM_058179.3:c.210T>A NP_478059.1:p.Tyr70Ter
NM_058179.4:c.210T>A MANE Select NP_478059.1:p.Tyr70Ter
NM_021154.5:c.210T>A NP_066977.1:p.Tyr70Ter
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