Canonical Allele Identifier: CA352000222

Gene: GLB1

Linked Data

• MyVariant Identifiers: chr3:g.33038643A>T (hg19) ; chr3:g.32997151A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32997151A>T , CM000665.2:g.32997151A>T	GRCh38
NC_000003.11:g.33038643A>T , CM000665.1:g.33038643A>T	GRCh37
NC_000003.10:g.33013647A>T	NCBI36
NG_009005.1:g.105052T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1928T>A MANE Select	ENSP00000306920.4:p.Val643Asp
ENST00000307363.9:c.1928T>A	ENSP00000306920.4:p.Val643Asp
ENST00000307377.12:c.1535T>A	ENSP00000305920.8:p.Val512Asp
ENST00000399402.7:c.1838T>A	ENSP00000382333.2:p.Val613Asp
NM_000404.2:c.1928T>A	NP_000395.2:p.Val643Asp
NM_000404.3:c.1928T>A	NP_000395.2:p.Val643Asp
NM_001079811.1:c.1838T>A	NP_001073279.1:p.Val613Asp
NM_001079811.2:c.1838T>A	NP_001073279.1:p.Val613Asp
NM_001135602.1:c.1535T>A	NP_001129074.1:p.Val512Asp
NM_001135602.2:c.1535T>A	NP_001129074.1:p.Val512Asp
NM_001317040.1:c.2072T>A	NP_001303969.1:p.Val691Asp
NM_000404.4:c.1928T>A MANE Select	NP_000395.3:p.Val643Asp
NM_001079811.3:c.1838T>A	NP_001073279.2:p.Val613Asp
NM_001135602.3:c.1535T>A	NP_001129074.2:p.Val512Asp
NM_001317040.2:c.2072T>A	NP_001303969.2:p.Val691Asp
NM_001393580.1:c.1734+16905T>A	NP_001380509.1:n.1734+16905T>A