Canonical Allele Identifier: CA351993157
Gene: GLB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021616A>C , CM000665.2:g.33021616A>C GRCh38
NC_000003.11:g.33063108A>C , CM000665.1:g.33063108A>C GRCh37
NC_000003.10:g.33038112A>C NCBI36
NG_009005.1:g.80587T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1183T>G MANE Select ENSP00000306920.4:p.Ser395Ala
ENST00000307363.9:c.1183T>G ENSP00000306920.4:p.Ser395Ala
ENST00000307377.12:c.790T>G ENSP00000305920.8:p.Ser264Ala
ENST00000399402.7:c.1093T>G ENSP00000382333.2:p.Ser365Ala
ENST00000461475.5:n.282T>G
ENST00000467571.5:n.220T>G
ENST00000473477.1:n.215T>G
ENST00000497796.5:n.435T>G
NM_000404.2:c.1183T>G NP_000395.2:p.Ser395Ala
NM_000404.3:c.1183T>G NP_000395.2:p.Ser395Ala
NM_001079811.1:c.1093T>G NP_001073279.1:p.Ser365Ala
NM_001079811.2:c.1093T>G NP_001073279.1:p.Ser365Ala
NM_001135602.1:c.790T>G NP_001129074.1:p.Ser264Ala
NM_001135602.2:c.790T>G NP_001129074.1:p.Ser264Ala
NM_001317040.1:c.1327T>G NP_001303969.1:p.Ser443Ala
XR_001740634.1:n.1543-572A>C
NM_000404.4:c.1183T>G MANE Select NP_000395.3:p.Ser395Ala
NM_001079811.3:c.1093T>G NP_001073279.2:p.Ser365Ala
NM_001135602.3:c.790T>G NP_001129074.2:p.Ser264Ala
NM_001317040.2:c.1327T>G NP_001303969.2:p.Ser443Ala
NM_001393580.1:c.1183T>G NP_001380509.1:p.Ser395Ala