Canonical Allele Identifier: CA2299649

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33058253C>T , CM000665.2:g.33058253C>T	GRCh38
NC_000003.11:g.33099745C>T , CM000665.1:g.33099745C>T	GRCh37
NC_000003.10:g.33074749C>T	NCBI36
NG_009005.1:g.43950G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.569G>A MANE Select	NP_000395.3:p.Gly190Asp
ENST00000307363.10:c.569G>A MANE Select	ENSP00000306920.4:p.Gly190Asp
NM_000404.2:c.569G>A	NP_000395.2:p.Gly190Asp
NM_000404.3:c.569G>A	NP_000395.2:p.Gly190Asp
NM_001079811.1:c.479G>A	NP_001073279.1:p.Gly160Asp
NM_001079811.2:c.479G>A	NP_001073279.1:p.Gly160Asp
NM_001079811.3:c.479G>A	NP_001073279.2:p.Gly160Asp
NM_001135602.1:c.341-4704G>A	NP_001129074.1:n.341-4704G>A
NM_001135602.2:c.341-4704G>A	NP_001129074.1:n.341-4704G>A
NM_001135602.3:c.341-4704G>A	NP_001129074.2:n.341-4704G>A
NM_001317040.1:c.713G>A	NP_001303969.1:p.Gly238Asp
NM_001317040.2:c.713G>A	NP_001303969.2:p.Gly238Asp
NM_001393580.1:c.569G>A	NP_001380509.1:p.Gly190Asp
ENST00000307363.9:c.569G>A	ENSP00000306920.4:p.Gly190Asp
ENST00000307377.12:c.341-4704G>A	ENSP00000305920.8:n.341-4704G>A
ENST00000399402.7:c.479G>A	ENSP00000382333.2:p.Gly160Asp
ENST00000415454.1:c.92G>A	ENSP00000411813.1:p.Gly31Asp
ENST00000438227.1:c.*61G>A	ENSP00000401250.1:n.*61G>A
ENST00000440656.1:c.176G>A	ENSP00000411769.1:p.Gly59Asp
ENST00000446732.5:c.*12G>A	ENSP00000407365.1:n.*12G>A
ENST00000482097.5:n.109-4704G>A
ENST00000485698.5:n.137-4704G>A
ENST00000498537.5:n.133-4704G>A