Canonical Allele Identifier: CA352001001
Community Standard Title: NM_000404.4(GLB1):c.931G>C (p.Gly311Arg)
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33051782C>G , CM000665.2:g.33051782C>G GRCh38
NC_000003.11:g.33093274C>G , CM000665.1:g.33093274C>G GRCh37
NC_000003.10:g.33068278C>G NCBI36
NG_009005.1:g.50421G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000404.4:c.931G>C MANE Select NP_000395.3:p.Gly311Arg
ENST00000307363.10:c.931G>C MANE Select ENSP00000306920.4:p.Gly311Arg
NM_000404.2:c.931G>C NP_000395.2:p.Gly311Arg
NM_000404.3:c.931G>C NP_000395.2:p.Gly311Arg
NM_001079811.1:c.841G>C NP_001073279.1:p.Gly281Arg
NM_001079811.2:c.841G>C NP_001073279.1:p.Gly281Arg
NM_001079811.3:c.841G>C NP_001073279.2:p.Gly281Arg
NM_001135602.1:c.538G>C NP_001129074.1:p.Gly180Arg
NM_001135602.2:c.538G>C NP_001129074.1:p.Gly180Arg
NM_001135602.3:c.538G>C NP_001129074.2:p.Gly180Arg
NM_001317040.1:c.1075G>C NP_001303969.1:p.Gly359Arg
NM_001317040.2:c.1075G>C NP_001303969.2:p.Gly359Arg
NM_001393580.1:c.931G>C NP_001380509.1:p.Gly311Arg
ENST00000307363.9:c.931G>C ENSP00000306920.4:p.Gly311Arg
ENST00000307377.12:c.538G>C ENSP00000305920.8:p.Gly180Arg
ENST00000399402.7:c.841G>C ENSP00000382333.2:p.Gly281Arg
ENST00000415454.1:c.454G>C ENSP00000411813.1:p.Gly152Arg
ENST00000482097.5:n.306G>C
ENST00000485698.5:n.334G>C
ENST00000498537.5:n.457G>C