Canonical Allele Identifier: CA1702659135
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41962086_41962105delinsCTCCAGGAAGGACAAAGCTG , CM000669.2:g.41962086_41962105delinsCTCCAGGAAGGACAAAGCTG GRCh38
NC_000007.13:g.42001684_42001703delinsCTCCAGGAAGGACAAAGCTG , CM000669.1:g.42001684_42001703delinsCTCCAGGAAGGACAAAGCTG GRCh37
NC_000007.12:g.41968209_41968228delinsCTCCAGGAAGGACAAAGCTG NCBI36
NG_008434.1:g.279916_279935delinsCAGCTTTGTCCTTCCTGGAG

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG MANE Select ENSP00000379258.3:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
ENST00000677288.1:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG ENSP00000503986.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
ENST00000677605.1:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG ENSP00000503743.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
ENST00000678429.1:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG ENSP00000502957.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
ENST00000395925.7:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG ENSP00000379258.3:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
NM_000168.5:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG NP_000159.3:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
XM_005249703.1:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG XP_005249760.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
XM_005249704.2:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG XP_005249761.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
XM_011515272.1:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG XP_011513574.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
XM_011515273.1:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG XP_011513575.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
XM_011515274.1:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG XP_011513576.1:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG
NM_000168.6:c.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG MANE Select NP_000159.3:n.*2225_*2244delinsCAGCTTTGTCCTTCCTGGAG