Canonical Allele Identifier: CA1702647512
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972228_41972229delinsAG , CM000669.2:g.41972228_41972229delinsAG GRCh38
NC_000007.13:g.42011827_42011828delinsAG , CM000669.1:g.42011827_42011828delinsAG GRCh37
NC_000007.12:g.41978352_41978353delinsAG NCBI36
NG_008434.1:g.269791_269792delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.2103+108_2103+109delinsCT MANE Select ENSP00000379258.3:n.2103+108_2103+109delinsCT
ENST00000677288.1:c.1929+108_1929+109delinsCT ENSP00000503986.1:n.1929+108_1929+109delinsCT
ENST00000677605.1:c.2103+108_2103+109delinsCT ENSP00000503743.1:n.2103+108_2103+109delinsCT
ENST00000678429.1:c.2103+108_2103+109delinsCT ENSP00000502957.1:n.2103+108_2103+109delinsCT
ENST00000395925.7:c.2103+108_2103+109delinsCT ENSP00000379258.3:n.2103+108_2103+109delinsCT
ENST00000479210.1:n.2080+108_2080+109delinsCT
NM_000168.5:c.2103+108_2103+109delinsCT NP_000159.3:n.2103+108_2103+109delinsCT
XM_005249703.1:c.2103+108_2103+109delinsCT XP_005249760.1:n.2103+108_2103+109delinsCT
XM_005249704.2:c.2103+108_2103+109delinsCT XP_005249761.1:n.2103+108_2103+109delinsCT
XM_011515272.1:c.2103+108_2103+109delinsCT XP_011513574.1:n.2103+108_2103+109delinsCT
XM_011515273.1:c.2103+108_2103+109delinsCT XP_011513575.1:n.2103+108_2103+109delinsCT
XM_011515274.1:c.1926+108_1926+109delinsCT XP_011513576.1:n.1926+108_1926+109delinsCT
XM_011515274.2:c.1926+108_1926+109delinsCT XP_011513576.1:n.1926+108_1926+109delinsCT
XM_017011997.1:c.2100+108_2100+109delinsCT XP_016867486.1:n.2100+108_2100+109delinsCT
NM_000168.6:c.2103+108_2103+109delinsCT MANE Select NP_000159.3:n.2103+108_2103+109delinsCT