Canonical Allele Identifier: CA1702659084
Gene: GLI3 HGNC NCBI

Linked Data

dbSNP Id: rs1787024452
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41961986_41961994dup , CM000669.2:g.41961986_41961994dup GRCh38
NC_000007.13:g.42001584_42001592dup , CM000669.1:g.42001584_42001592dup GRCh37
NC_000007.12:g.41968109_41968117dup NCBI36
NG_008434.1:g.280034_280042dup

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.*2343_*2351dup MANE Select ENSP00000379258.3:n.*2343_*2351dup
ENST00000677288.1:c.*2343_*2351dup ENSP00000503986.1:n.*2343_*2351dup
ENST00000677605.1:c.*2343_*2351dup ENSP00000503743.1:n.*2343_*2351dup
ENST00000678429.1:c.*2343_*2351dup ENSP00000502957.1:n.*2343_*2351dup
ENST00000395925.7:c.*2343_*2351dup ENSP00000379258.3:n.*2343_*2351dup
NM_000168.5:c.*2343_*2351dup NP_000159.3:n.*2343_*2351dup
XM_005249703.1:c.*2343_*2351dup XP_005249760.1:n.*2343_*2351dup
XM_005249704.2:c.*2343_*2351dup XP_005249761.1:n.*2343_*2351dup
XM_011515272.1:c.*2343_*2351dup XP_011513574.1:n.*2343_*2351dup
XM_011515273.1:c.*2343_*2351dup XP_011513575.1:n.*2343_*2351dup
XM_011515274.1:c.*2343_*2351dup XP_011513576.1:n.*2343_*2351dup
NM_000168.6:c.*2343_*2351dup MANE Select NP_000159.3:n.*2343_*2351dup
Search 100 bp 5'
Search 100 bp 3'