Canonical Allele Identifier: CA1355976995
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997347_32997351delinsGGAGA , CM000665.2:g.32997347_32997351delinsGGAGA GRCh38
NC_000003.11:g.33038839_33038843delinsGGAGA , CM000665.1:g.33038839_33038843delinsGGAGA GRCh37
NC_000003.10:g.33013843_33013847delinsGGAGA NCBI36
NG_009005.1:g.104852_104856delinsTCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1735-7_1735-3delinsTCTCC MANE Select ENSP00000306920.4:n.1735-7_1735-3delinsTCTCC
ENST00000307363.9:c.1735-7_1735-3delinsTCTCC ENSP00000306920.4:n.1735-7_1735-3delinsTCTCC
ENST00000307377.12:c.1342-7_1342-3delinsTCTCC ENSP00000305920.8:n.1342-7_1342-3delinsTCTCC
ENST00000399402.7:c.1645-7_1645-3delinsTCTCC ENSP00000382333.2:n.1645-7_1645-3delinsTCTCC
NM_000404.2:c.1735-7_1735-3delinsTCTCC NP_000395.2:n.1735-7_1735-3delinsTCTCC
NM_000404.3:c.1735-7_1735-3delinsTCTCC NP_000395.2:n.1735-7_1735-3delinsTCTCC
NM_001079811.1:c.1645-7_1645-3delinsTCTCC NP_001073279.1:n.1645-7_1645-3delinsTCTCC
NM_001079811.2:c.1645-7_1645-3delinsTCTCC NP_001073279.1:n.1645-7_1645-3delinsTCTCC
NM_001135602.1:c.1342-7_1342-3delinsTCTCC NP_001129074.1:n.1342-7_1342-3delinsTCTCC
NM_001135602.2:c.1342-7_1342-3delinsTCTCC NP_001129074.1:n.1342-7_1342-3delinsTCTCC
NM_001317040.1:c.1879-7_1879-3delinsTCTCC NP_001303969.1:n.1879-7_1879-3delinsTCTCC
NM_000404.4:c.1735-7_1735-3delinsTCTCC MANE Select NP_000395.3:n.1735-7_1735-3delinsTCTCC
NM_001079811.3:c.1645-7_1645-3delinsTCTCC NP_001073279.2:n.1645-7_1645-3delinsTCTCC
NM_001135602.3:c.1342-7_1342-3delinsTCTCC NP_001129074.2:n.1342-7_1342-3delinsTCTCC
NM_001317040.2:c.1879-7_1879-3delinsTCTCC NP_001303969.2:n.1879-7_1879-3delinsTCTCC
NM_001393580.1:c.1734+16705_1734+16709delinsTCTCC NP_001380509.1:n.1734+16705_1734+16709delinsTCTCC