Canonical Allele Identifier: CA2299524
Community Standard Title: NM_000404.4(GLB1):c.998A>G (p.Tyr333Cys)
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33046190T>C , CM000665.2:g.33046190T>C GRCh38
NC_000003.11:g.33087682T>C , CM000665.1:g.33087682T>C GRCh37
NC_000003.10:g.33062686T>C NCBI36
NG_009005.1:g.56013A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000404.4:c.998A>G MANE Select NP_000395.3:p.Tyr333Cys
ENST00000307363.10:c.998A>G MANE Select ENSP00000306920.4:p.Tyr333Cys
NM_000404.2:c.998A>G NP_000395.2:p.Tyr333Cys
NM_000404.3:c.998A>G NP_000395.2:p.Tyr333Cys
NM_001079811.1:c.908A>G NP_001073279.1:p.Tyr303Cys
NM_001079811.2:c.908A>G NP_001073279.1:p.Tyr303Cys
NM_001079811.3:c.908A>G NP_001073279.2:p.Tyr303Cys
NM_001135602.1:c.605A>G NP_001129074.1:p.Tyr202Cys
NM_001135602.2:c.605A>G NP_001129074.1:p.Tyr202Cys
NM_001135602.3:c.605A>G NP_001129074.2:p.Tyr202Cys
NM_001317040.1:c.1142A>G NP_001303969.1:p.Tyr381Cys
NM_001317040.2:c.1142A>G NP_001303969.2:p.Tyr381Cys
NM_001393580.1:c.998A>G NP_001380509.1:p.Tyr333Cys
ENST00000307363.9:c.998A>G ENSP00000306920.4:p.Tyr333Cys
ENST00000307377.12:c.605A>G ENSP00000305920.8:p.Tyr202Cys
ENST00000399402.7:c.908A>G ENSP00000382333.2:p.Tyr303Cys
ENST00000415454.1:c.521A>G ENSP00000411813.1:p.Tyr174Cys
ENST00000482097.5:n.373A>G
ENST00000485698.5:n.401A>G
ENST00000490658.2:n.3A>G
ENST00000498537.5:n.524A>G