Canonical Allele Identifier: CA352004014

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33099619G>C (hg19) ; chr3:g.33058127G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33058127G>C , CM000665.2:g.33058127G>C	GRCh38
NC_000003.11:g.33099619G>C , CM000665.1:g.33099619G>C	GRCh37
NC_000003.10:g.33074623G>C	NCBI36
NG_009005.1:g.44076C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.695C>G MANE Select	ENSP00000306920.4:p.Ala232Gly
ENST00000307363.9:c.695C>G	ENSP00000306920.4:p.Ala232Gly
ENST00000307377.12:c.341-4578C>G	ENSP00000305920.8:n.341-4578C>G
ENST00000399402.7:c.605C>G	ENSP00000382333.2:p.Ala202Gly
ENST00000415454.1:c.218C>G	ENSP00000411813.1:p.Ala73Gly
ENST00000438227.1:c.*187C>G	ENSP00000401250.1:n.*187C>G
ENST00000440656.1:c.302C>G	ENSP00000411769.1:p.Ala101Gly
ENST00000446732.5:c.*138C>G	ENSP00000407365.1:n.*138C>G
ENST00000482097.5:n.109-4578C>G
ENST00000485698.5:n.137-4578C>G
ENST00000498537.5:n.133-4578C>G
NM_000404.2:c.695C>G	NP_000395.2:p.Ala232Gly
NM_000404.3:c.695C>G	NP_000395.2:p.Ala232Gly
NM_001079811.1:c.605C>G	NP_001073279.1:p.Ala202Gly
NM_001079811.2:c.605C>G	NP_001073279.1:p.Ala202Gly
NM_001135602.1:c.341-4578C>G	NP_001129074.1:n.341-4578C>G
NM_001135602.2:c.341-4578C>G	NP_001129074.1:n.341-4578C>G
NM_001317040.1:c.839C>G	NP_001303969.1:p.Ala280Gly
NM_000404.4:c.695C>G MANE Select	NP_000395.3:p.Ala232Gly
NM_001079811.3:c.605C>G	NP_001073279.2:p.Ala202Gly
NM_001135602.3:c.341-4578C>G	NP_001129074.2:n.341-4578C>G
NM_001317040.2:c.839C>G	NP_001303969.2:p.Ala280Gly
NM_001393580.1:c.695C>G	NP_001380509.1:p.Ala232Gly