Canonical Allele Identifier: CA1702775548
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.42236993G= , CM000669.2:g.42236993G= GRCh38
NC_000007.13:g.42276592G= , CM000669.1:g.42276592G= GRCh37
NC_000007.12:g.42243117G= NCBI36
NG_008434.1:g.5027C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.-65C= MANE Select ENSP00000379258.3:n.-65C=
ENST00000428534.2:c.-43+791C= ENSP00000503957.1:n.-43+791C=
ENST00000677605.1:c.-43+506C= ENSP00000503743.1:n.-43+506C=
ENST00000677990.1:n.217C=
ENST00000678978.1:c.-42-13698C= ENSP00000503352.1:n.-42-13698C=
ENST00000395925.7:c.-65C= ENSP00000379258.3:n.-65C=
ENST00000428534.1:n.87+791C=
ENST00000437480.1:c.-65C= ENSP00000407963.1:n.-65C=
NM_000168.5:c.-65C= NP_000159.3:n.-65C=
XM_005249703.1:c.-43+791C= XP_005249760.1:n.-43+791C=
XM_005249704.2:c.-43+506C= XP_005249761.1:n.-43+506C=
XM_011515273.1:c.-42-13698C= XP_011513575.1:n.-42-13698C=
NM_000168.6:c.-65C= MANE Select NP_000159.3:n.-65C=