Canonical Allele Identifier: CA351992851
Gene: GLB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021574C>G , CM000665.2:g.33021574C>G GRCh38
NC_000003.11:g.33063066C>G , CM000665.1:g.33063066C>G GRCh37
NC_000003.10:g.33038070C>G NCBI36
NG_009005.1:g.80629G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1225G>C MANE Select ENSP00000306920.4:p.Val409Leu
ENST00000307363.9:c.1225G>C ENSP00000306920.4:p.Val409Leu
ENST00000307377.12:c.832G>C ENSP00000305920.8:p.Val278Leu
ENST00000399402.7:c.1135G>C ENSP00000382333.2:p.Val379Leu
ENST00000461475.5:n.324G>C
ENST00000467571.5:n.262G>C
ENST00000473477.1:n.257G>C
ENST00000497796.5:n.477G>C
NM_000404.2:c.1225G>C NP_000395.2:p.Val409Leu
NM_000404.3:c.1225G>C NP_000395.2:p.Val409Leu
NM_001079811.1:c.1135G>C NP_001073279.1:p.Val379Leu
NM_001079811.2:c.1135G>C NP_001073279.1:p.Val379Leu
NM_001135602.1:c.832G>C NP_001129074.1:p.Val278Leu
NM_001135602.2:c.832G>C NP_001129074.1:p.Val278Leu
NM_001317040.1:c.1369G>C NP_001303969.1:p.Val457Leu
XR_001740634.1:n.1543-614C>G
NM_000404.4:c.1225G>C MANE Select NP_000395.3:p.Val409Leu
NM_001079811.3:c.1135G>C NP_001073279.2:p.Val379Leu
NM_001135602.3:c.832G>C NP_001129074.2:p.Val278Leu
NM_001317040.2:c.1369G>C NP_001303969.2:p.Val457Leu
NM_001393580.1:c.1225G>C NP_001380509.1:p.Val409Leu