Canonical Allele Identifier: CA2299701
Community Standard Title: NM_000404.4(GLB1):c.446C>T (p.Ser149Phe)
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33068241G>A , CM000665.2:g.33068241G>A GRCh38
NC_000003.11:g.33109733G>A , CM000665.1:g.33109733G>A GRCh37
NC_000003.10:g.33084737G>A NCBI36
NG_009005.1:g.33962C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000404.4:c.446C>T MANE Select NP_000395.3:p.Ser149Phe
ENST00000307363.10:c.446C>T MANE Select ENSP00000306920.4:p.Ser149Phe
NM_000404.2:c.446C>T NP_000395.2:p.Ser149Phe
NM_000404.3:c.446C>T NP_000395.2:p.Ser149Phe
NM_001079811.1:c.356C>T NP_001073279.1:p.Ser119Phe
NM_001079811.2:c.356C>T NP_001073279.1:p.Ser119Phe
NM_001079811.3:c.356C>T NP_001073279.2:p.Ser119Phe
NM_001135602.1:c.246-2684C>T NP_001129074.1:n.246-2684C>T
NM_001135602.2:c.246-2684C>T NP_001129074.1:n.246-2684C>T
NM_001135602.3:c.246-2684C>T NP_001129074.2:n.246-2684C>T
NM_001317040.1:c.590C>T NP_001303969.1:p.Ser197Phe
NM_001317040.2:c.590C>T NP_001303969.2:p.Ser197Phe
NM_001393580.1:c.446C>T NP_001380509.1:p.Ser149Phe
ENST00000307363.9:c.446C>T ENSP00000306920.4:p.Ser149Phe
ENST00000307377.12:c.246-2684C>T ENSP00000305920.8:n.246-2684C>T
ENST00000399402.7:c.356C>T ENSP00000382333.2:p.Ser119Phe
ENST00000415454.1:c.76-9972C>T ENSP00000411813.1:n.76-9972C>T
ENST00000438227.1:c.76-2684C>T ENSP00000401250.1:n.76-2684C>T
ENST00000440656.1:c.53C>T ENSP00000411769.1:p.Ser18Phe
ENST00000446732.5:c.156-2684C>T ENSP00000407365.1:n.156-2684C>T
ENST00000464355.1:n.404C>T
ENST00000482097.5:n.109-14692C>T
ENST00000485698.5:n.137-14692C>T
ENST00000498537.5:n.133-14692C>T