Canonical Allele Identifier: CA352000994

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33051781C>T , CM000665.2:g.33051781C>T	GRCh38
NC_000003.11:g.33093273C>T , CM000665.1:g.33093273C>T	GRCh37
NC_000003.10:g.33068277C>T	NCBI36
NG_009005.1:g.50422G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.932G>A MANE Select	NP_000395.3:p.Gly311Glu
ENST00000307363.10:c.932G>A MANE Select	ENSP00000306920.4:p.Gly311Glu
NM_000404.2:c.932G>A	NP_000395.2:p.Gly311Glu
NM_000404.3:c.932G>A	NP_000395.2:p.Gly311Glu
NM_001079811.1:c.842G>A	NP_001073279.1:p.Gly281Glu
NM_001079811.2:c.842G>A	NP_001073279.1:p.Gly281Glu
NM_001079811.3:c.842G>A	NP_001073279.2:p.Gly281Glu
NM_001135602.1:c.539G>A	NP_001129074.1:p.Gly180Glu
NM_001135602.2:c.539G>A	NP_001129074.1:p.Gly180Glu
NM_001135602.3:c.539G>A	NP_001129074.2:p.Gly180Glu
NM_001317040.1:c.1076G>A	NP_001303969.1:p.Gly359Glu
NM_001317040.2:c.1076G>A	NP_001303969.2:p.Gly359Glu
NM_001393580.1:c.932G>A	NP_001380509.1:p.Gly311Glu
ENST00000307363.9:c.932G>A	ENSP00000306920.4:p.Gly311Glu
ENST00000307377.12:c.539G>A	ENSP00000305920.8:p.Gly180Glu
ENST00000399402.7:c.842G>A	ENSP00000382333.2:p.Gly281Glu
ENST00000415454.1:c.455G>A	ENSP00000411813.1:p.Gly152Glu
ENST00000482097.5:n.307G>A
ENST00000485698.5:n.335G>A
ENST00000498537.5:n.458G>A