Canonical Allele Identifier: CA1702691737
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.42040439_42040440delinsCG , CM000669.2:g.42040439_42040440delinsCG GRCh38
NC_000007.13:g.42080038_42080039delinsCG , CM000669.1:g.42080038_42080039delinsCG GRCh37
NC_000007.12:g.42046563_42046564delinsCG NCBI36
NG_008434.1:g.201580_201581delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.827-201_827-200delinsCG MANE Select ENSP00000379258.3:n.827-201_827-200delinsCG
ENST00000677288.1:c.650-201_650-200delinsCG ENSP00000503986.1:n.650-201_650-200delinsCG
ENST00000677605.1:c.827-201_827-200delinsCG ENSP00000503743.1:n.827-201_827-200delinsCG
ENST00000678429.1:c.827-201_827-200delinsCG ENSP00000502957.1:n.827-201_827-200delinsCG
ENST00000395925.7:c.827-201_827-200delinsCG ENSP00000379258.3:n.827-201_827-200delinsCG
ENST00000479210.1:n.804-201_804-200delinsCG
NM_000168.5:c.827-201_827-200delinsCG NP_000159.3:n.827-201_827-200delinsCG
XM_005249703.1:c.827-201_827-200delinsCG XP_005249760.1:n.827-201_827-200delinsCG
XM_005249704.2:c.827-201_827-200delinsCG XP_005249761.1:n.827-201_827-200delinsCG
XM_011515272.1:c.827-201_827-200delinsCG XP_011513574.1:n.827-201_827-200delinsCG
XM_011515273.1:c.827-201_827-200delinsCG XP_011513575.1:n.827-201_827-200delinsCG
XM_011515274.1:c.650-201_650-200delinsCG XP_011513576.1:n.650-201_650-200delinsCG
XM_011515274.2:c.650-201_650-200delinsCG XP_011513576.1:n.650-201_650-200delinsCG
XM_017011997.1:c.824-201_824-200delinsCG XP_016867486.1:n.824-201_824-200delinsCG
NM_000168.6:c.827-201_827-200delinsCG MANE Select NP_000159.3:n.827-201_827-200delinsCG