Canonical Allele Identifier: CA351993101
Gene: GLB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021607T>G , CM000665.2:g.33021607T>G GRCh38
NC_000003.11:g.33063099T>G , CM000665.1:g.33063099T>G GRCh37
NC_000003.10:g.33038103T>G NCBI36
NG_009005.1:g.80596A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1192A>C MANE Select ENSP00000306920.4:p.Ile398Leu
ENST00000307363.9:c.1192A>C ENSP00000306920.4:p.Ile398Leu
ENST00000307377.12:c.799A>C ENSP00000305920.8:p.Ile267Leu
ENST00000399402.7:c.1102A>C ENSP00000382333.2:p.Ile368Leu
ENST00000461475.5:n.291A>C
ENST00000467571.5:n.229A>C
ENST00000473477.1:n.224A>C
ENST00000497796.5:n.444A>C
NM_000404.2:c.1192A>C NP_000395.2:p.Ile398Leu
NM_000404.3:c.1192A>C NP_000395.2:p.Ile398Leu
NM_001079811.1:c.1102A>C NP_001073279.1:p.Ile368Leu
NM_001079811.2:c.1102A>C NP_001073279.1:p.Ile368Leu
NM_001135602.1:c.799A>C NP_001129074.1:p.Ile267Leu
NM_001135602.2:c.799A>C NP_001129074.1:p.Ile267Leu
NM_001317040.1:c.1336A>C NP_001303969.1:p.Ile446Leu
XR_001740634.1:n.1543-581T>G
NM_000404.4:c.1192A>C MANE Select NP_000395.3:p.Ile398Leu
NM_001079811.3:c.1102A>C NP_001073279.2:p.Ile368Leu
NM_001135602.3:c.799A>C NP_001129074.2:p.Ile267Leu
NM_001317040.2:c.1336A>C NP_001303969.2:p.Ile446Leu
NM_001393580.1:c.1192A>C NP_001380509.1:p.Ile398Leu