Canonical Allele Identifier: CA2775168839
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41963390dup , CM000669.2:g.41963390dup GRCh38
NC_000007.13:g.42002988dup , CM000669.1:g.42002988dup GRCh37
NC_000007.12:g.41969513dup NCBI36
NG_008434.1:g.278631dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.*940dup MANE Select ENSP00000379258.3:n.*940dup
ENST00000677288.1:c.*940dup ENSP00000503986.1:n.*940dup
ENST00000677605.1:c.*940dup ENSP00000503743.1:n.*940dup
ENST00000678429.1:c.*940dup ENSP00000502957.1:n.*940dup
ENST00000395925.7:c.*940dup ENSP00000379258.3:n.*940dup
NM_000168.5:c.*940dup NP_000159.3:n.*940dup
XM_005249703.1:c.*940dup XP_005249760.1:n.*940dup
XM_005249704.2:c.*940dup XP_005249761.1:n.*940dup
XM_011515272.1:c.*940dup XP_011513574.1:n.*940dup
XM_011515273.1:c.*940dup XP_011513575.1:n.*940dup
XM_011515274.1:c.*940dup XP_011513576.1:n.*940dup
NM_000168.6:c.*940dup MANE Select NP_000159.3:n.*940dup