Canonical Allele Identifier: CA1356003791
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33058122G= , CM000665.2:g.33058122G= GRCh38
NC_000003.11:g.33099614G= , CM000665.1:g.33099614G= GRCh37
NC_000003.10:g.33074618G= NCBI36
NG_009005.1:g.44081C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.700C= MANE Select ENSP00000306920.4:p.Gln234=
ENST00000307363.9:c.700C= ENSP00000306920.4:p.Gln234=
ENST00000307377.12:c.341-4573C= ENSP00000305920.8:n.341-4573C=
ENST00000399402.7:c.610C= ENSP00000382333.2:p.Gln204=
ENST00000415454.1:c.223C= ENSP00000411813.1:p.Gln75=
ENST00000438227.1:c.*192C= ENSP00000401250.1:n.*192C=
ENST00000440656.1:c.307C= ENSP00000411769.1:p.Gln103=
ENST00000446732.5:c.*143C= ENSP00000407365.1:n.*143C=
ENST00000482097.5:n.109-4573C=
ENST00000485698.5:n.137-4573C=
ENST00000498537.5:n.133-4573C=
NM_000404.2:c.700C= NP_000395.2:p.Gln234=
NM_000404.3:c.700C= NP_000395.2:p.Gln234=
NM_001079811.1:c.610C= NP_001073279.1:p.Gln204=
NM_001079811.2:c.610C= NP_001073279.1:p.Gln204=
NM_001135602.1:c.341-4573C= NP_001129074.1:n.341-4573C=
NM_001135602.2:c.341-4573C= NP_001129074.1:n.341-4573C=
NM_001317040.1:c.844C= NP_001303969.1:p.Gln282=
NM_000404.4:c.700C= MANE Select NP_000395.3:p.Gln234=
NM_001079811.3:c.610C= NP_001073279.2:p.Gln204=
NM_001135602.3:c.341-4573C= NP_001129074.2:n.341-4573C=
NM_001317040.2:c.844C= NP_001303969.2:p.Gln282=
NM_001393580.1:c.700C= NP_001380509.1:p.Gln234=