Canonical Allele Identifier: CA1702647542
Gene: GLI3 HGNC NCBI

Linked Data

dbSNP Id: rs1787382906

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972269_41972270insA , CM000669.2:g.41972269_41972270insA GRCh38
NC_000007.13:g.42011868_42011869insA , CM000669.1:g.42011868_42011869insA GRCh37
NC_000007.12:g.41978393_41978394insA NCBI36
NG_008434.1:g.269750_269751insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.2103+67_2103+68insT MANE Select ENSP00000379258.3:n.2103+67_2103+68insT
ENST00000677288.1:c.1929+67_1929+68insT ENSP00000503986.1:n.1929+67_1929+68insT
ENST00000677605.1:c.2103+67_2103+68insT ENSP00000503743.1:n.2103+67_2103+68insT
ENST00000678429.1:c.2103+67_2103+68insT ENSP00000502957.1:n.2103+67_2103+68insT
ENST00000395925.7:c.2103+67_2103+68insT ENSP00000379258.3:n.2103+67_2103+68insT
ENST00000479210.1:n.2080+67_2080+68insT
NM_000168.5:c.2103+67_2103+68insT NP_000159.3:n.2103+67_2103+68insT
XM_005249703.1:c.2103+67_2103+68insT XP_005249760.1:n.2103+67_2103+68insT
XM_005249704.2:c.2103+67_2103+68insT XP_005249761.1:n.2103+67_2103+68insT
XM_011515272.1:c.2103+67_2103+68insT XP_011513574.1:n.2103+67_2103+68insT
XM_011515273.1:c.2103+67_2103+68insT XP_011513575.1:n.2103+67_2103+68insT
XM_011515274.1:c.1926+67_1926+68insT XP_011513576.1:n.1926+67_1926+68insT
XM_011515274.2:c.1926+67_1926+68insT XP_011513576.1:n.1926+67_1926+68insT
XM_017011997.1:c.2100+67_2100+68insT XP_016867486.1:n.2100+67_2100+68insT
NM_000168.6:c.2103+67_2103+68insT MANE Select NP_000159.3:n.2103+67_2103+68insT