Canonical Allele Identifier: CA1702647459
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972162_41972163delinsCT , CM000669.2:g.41972162_41972163delinsCT GRCh38
NC_000007.13:g.42011761_42011762delinsCT , CM000669.1:g.42011761_42011762delinsCT GRCh37
NC_000007.12:g.41978286_41978287delinsCT NCBI36
NG_008434.1:g.269857_269858delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395925.8:c.2103+174_2103+175delinsAG MANE Select ENSP00000379258.3:n.2103+174_2103+175delinsAG
ENST00000677288.1:c.1929+174_1929+175delinsAG ENSP00000503986.1:n.1929+174_1929+175delinsAG
ENST00000677605.1:c.2103+174_2103+175delinsAG ENSP00000503743.1:n.2103+174_2103+175delinsAG
ENST00000678429.1:c.2103+174_2103+175delinsAG ENSP00000502957.1:n.2103+174_2103+175delinsAG
ENST00000395925.7:c.2103+174_2103+175delinsAG ENSP00000379258.3:n.2103+174_2103+175delinsAG
ENST00000479210.1:n.2080+174_2080+175delinsAG
NM_000168.5:c.2103+174_2103+175delinsAG NP_000159.3:n.2103+174_2103+175delinsAG
XM_005249703.1:c.2103+174_2103+175delinsAG XP_005249760.1:n.2103+174_2103+175delinsAG
XM_005249704.2:c.2103+174_2103+175delinsAG XP_005249761.1:n.2103+174_2103+175delinsAG
XM_011515272.1:c.2103+174_2103+175delinsAG XP_011513574.1:n.2103+174_2103+175delinsAG
XM_011515273.1:c.2103+174_2103+175delinsAG XP_011513575.1:n.2103+174_2103+175delinsAG
XM_011515274.1:c.1926+174_1926+175delinsAG XP_011513576.1:n.1926+174_1926+175delinsAG
XM_011515274.2:c.1926+174_1926+175delinsAG XP_011513576.1:n.1926+174_1926+175delinsAG
XM_017011997.1:c.2100+174_2100+175delinsAG XP_016867486.1:n.2100+174_2100+175delinsAG
NM_000168.6:c.2103+174_2103+175delinsAG MANE Select NP_000159.3:n.2103+174_2103+175delinsAG