Canonical Allele Identifier: CA1355977017
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32997404_32997405delinsTG , CM000665.2:g.32997404_32997405delinsTG GRCh38
NC_000003.11:g.33038896_33038897delinsTG , CM000665.1:g.33038896_33038897delinsTG GRCh37
NC_000003.10:g.33013900_33013901delinsTG NCBI36
NG_009005.1:g.104798_104799delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1735-61_1735-60delinsCA MANE Select ENSP00000306920.4:n.1735-61_1735-60delinsCA
ENST00000307363.9:c.1735-61_1735-60delinsCA ENSP00000306920.4:n.1735-61_1735-60delinsCA
ENST00000307377.12:c.1342-61_1342-60delinsCA ENSP00000305920.8:n.1342-61_1342-60delinsCA
ENST00000399402.7:c.1645-61_1645-60delinsCA ENSP00000382333.2:n.1645-61_1645-60delinsCA
NM_000404.2:c.1735-61_1735-60delinsCA NP_000395.2:n.1735-61_1735-60delinsCA
NM_000404.3:c.1735-61_1735-60delinsCA NP_000395.2:n.1735-61_1735-60delinsCA
NM_001079811.1:c.1645-61_1645-60delinsCA NP_001073279.1:n.1645-61_1645-60delinsCA
NM_001079811.2:c.1645-61_1645-60delinsCA NP_001073279.1:n.1645-61_1645-60delinsCA
NM_001135602.1:c.1342-61_1342-60delinsCA NP_001129074.1:n.1342-61_1342-60delinsCA
NM_001135602.2:c.1342-61_1342-60delinsCA NP_001129074.1:n.1342-61_1342-60delinsCA
NM_001317040.1:c.1879-61_1879-60delinsCA NP_001303969.1:n.1879-61_1879-60delinsCA
NM_000404.4:c.1735-61_1735-60delinsCA MANE Select NP_000395.3:n.1735-61_1735-60delinsCA
NM_001079811.3:c.1645-61_1645-60delinsCA NP_001073279.2:n.1645-61_1645-60delinsCA
NM_001135602.3:c.1342-61_1342-60delinsCA NP_001129074.2:n.1342-61_1342-60delinsCA
NM_001317040.2:c.1879-61_1879-60delinsCA NP_001303969.2:n.1879-61_1879-60delinsCA
NM_001393580.1:c.1734+16651_1734+16652delinsCA NP_001380509.1:n.1734+16651_1734+16652delinsCA