Canonical Allele Identifier: CA373872015
Gene: PSAT1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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