Canonical Allele Identifier: CA2682510153
Gene: GLI3 HGNC NCBI

Linked Data

dbSNP Id: rs2128709871

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972317_41972319del , CM000669.2:g.41972317_41972319del GRCh38
NC_000007.13:g.42011916_42011918del , CM000669.1:g.42011916_42011918del GRCh37
NC_000007.12:g.41978441_41978443del NCBI36
NG_008434.1:g.269703_269705del

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.2103+20_2103+22del MANE Select ENSP00000379258.3:n.2103+20_2103+22del
ENST00000677288.1:c.1929+20_1929+22del ENSP00000503986.1:n.1929+20_1929+22del
ENST00000677605.1:c.2103+20_2103+22del ENSP00000503743.1:n.2103+20_2103+22del
ENST00000678429.1:c.2103+20_2103+22del ENSP00000502957.1:n.2103+20_2103+22del
ENST00000395925.7:c.2103+20_2103+22del ENSP00000379258.3:n.2103+20_2103+22del
ENST00000479210.1:n.2080+20_2080+22del
NM_000168.5:c.2103+20_2103+22del NP_000159.3:n.2103+20_2103+22del
XM_005249703.1:c.2103+20_2103+22del XP_005249760.1:n.2103+20_2103+22del
XM_005249704.2:c.2103+20_2103+22del XP_005249761.1:n.2103+20_2103+22del
XM_011515272.1:c.2103+20_2103+22del XP_011513574.1:n.2103+20_2103+22del
XM_011515273.1:c.2103+20_2103+22del XP_011513575.1:n.2103+20_2103+22del
XM_011515274.1:c.1926+20_1926+22del XP_011513576.1:n.1926+20_1926+22del
XM_011515274.2:c.1926+20_1926+22del XP_011513576.1:n.1926+20_1926+22del
XM_017011997.1:c.2100+20_2100+22del XP_016867486.1:n.2100+20_2100+22del
NM_000168.6:c.2103+20_2103+22del MANE Select NP_000159.3:n.2103+20_2103+22del