Canonical Allele Identifier: CA351999176

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33046128T>C , CM000665.2:g.33046128T>C	GRCh38
NC_000003.11:g.33087620T>C , CM000665.1:g.33087620T>C	GRCh37
NC_000003.10:g.33062624T>C	NCBI36
NG_009005.1:g.56075A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000404.4:c.1060A>G MANE Select	NP_000395.3:p.Ile354Val
ENST00000307363.10:c.1060A>G MANE Select	ENSP00000306920.4:p.Ile354Val
NM_000404.2:c.1060A>G	NP_000395.2:p.Ile354Val
NM_000404.3:c.1060A>G	NP_000395.2:p.Ile354Val
NM_001079811.1:c.970A>G	NP_001073279.1:p.Ile324Val
NM_001079811.2:c.970A>G	NP_001073279.1:p.Ile324Val
NM_001079811.3:c.970A>G	NP_001073279.2:p.Ile324Val
NM_001135602.1:c.667A>G	NP_001129074.1:p.Ile223Val
NM_001135602.2:c.667A>G	NP_001129074.1:p.Ile223Val
NM_001135602.3:c.667A>G	NP_001129074.2:p.Ile223Val
NM_001317040.1:c.1204A>G	NP_001303969.1:p.Ile402Val
NM_001317040.2:c.1204A>G	NP_001303969.2:p.Ile402Val
NM_001393580.1:c.1060A>G	NP_001380509.1:p.Ile354Val
ENST00000307363.9:c.1060A>G	ENSP00000306920.4:p.Ile354Val
ENST00000307377.12:c.667A>G	ENSP00000305920.8:p.Ile223Val
ENST00000399402.7:c.970A>G	ENSP00000382333.2:p.Ile324Val
ENST00000482097.5:n.435A>G
ENST00000485698.5:n.463A>G
ENST00000490658.2:n.65A>G