Canonical Allele Identifier: CA10604067
Gene: GLI3 HGNC NCBI

Linked Data

ClinVar Variation Id: 282092
ClinVar RCV Id: RCV000347627
dbSNP Id: rs886042309

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41964724A>C , CM000669.2:g.41964724A>C GRCh38
NC_000007.13:g.42004322A>C , CM000669.1:g.42004322A>C GRCh37
NC_000007.12:g.41970847A>C NCBI36
NG_008434.1:g.277297T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.4349T>G MANE Select ENSP00000379258.3:p.Phe1450Cys
ENST00000677288.1:c.4175T>G ENSP00000503986.1:p.Phe1392Cys
ENST00000677605.1:c.4349T>G ENSP00000503743.1:p.Phe1450Cys
ENST00000678429.1:c.4349T>G ENSP00000502957.1:p.Phe1450Cys
ENST00000395925.7:c.4349T>G ENSP00000379258.3:p.Phe1450Cys
ENST00000479210.1:n.4326T>G
NM_000168.5:c.4349T>G NP_000159.3:p.Phe1450Cys
XM_005249703.1:c.4349T>G XP_005249760.1:p.Phe1450Cys
XM_005249704.2:c.4349T>G XP_005249761.1:p.Phe1450Cys
XM_011515272.1:c.4349T>G XP_011513574.1:p.Phe1450Cys
XM_011515273.1:c.4349T>G XP_011513575.1:p.Phe1450Cys
XM_011515274.1:c.4172T>G XP_011513576.1:p.Phe1391Cys
XM_011515274.2:c.4172T>G XP_011513576.1:p.Phe1391Cys
XM_017011997.1:c.4346T>G XP_016867486.1:p.Phe1449Cys
NM_000168.6:c.4349T>G MANE Select NP_000159.3:p.Phe1450Cys