Canonical Allele Identifier: CA1702647531
Gene: GLI3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41972260_41972261delinsTC , CM000669.2:g.41972260_41972261delinsTC GRCh38
NC_000007.13:g.42011859_42011860delinsTC , CM000669.1:g.42011859_42011860delinsTC GRCh37
NC_000007.12:g.41978384_41978385delinsTC NCBI36
NG_008434.1:g.269759_269760delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000395925.8:c.2103+76_2103+77delinsGA MANE Select ENSP00000379258.3:n.2103+76_2103+77delinsGA
ENST00000677288.1:c.1929+76_1929+77delinsGA ENSP00000503986.1:n.1929+76_1929+77delinsGA
ENST00000677605.1:c.2103+76_2103+77delinsGA ENSP00000503743.1:n.2103+76_2103+77delinsGA
ENST00000678429.1:c.2103+76_2103+77delinsGA ENSP00000502957.1:n.2103+76_2103+77delinsGA
ENST00000395925.7:c.2103+76_2103+77delinsGA ENSP00000379258.3:n.2103+76_2103+77delinsGA
ENST00000479210.1:n.2080+76_2080+77delinsGA
NM_000168.5:c.2103+76_2103+77delinsGA NP_000159.3:n.2103+76_2103+77delinsGA
XM_005249703.1:c.2103+76_2103+77delinsGA XP_005249760.1:n.2103+76_2103+77delinsGA
XM_005249704.2:c.2103+76_2103+77delinsGA XP_005249761.1:n.2103+76_2103+77delinsGA
XM_011515272.1:c.2103+76_2103+77delinsGA XP_011513574.1:n.2103+76_2103+77delinsGA
XM_011515273.1:c.2103+76_2103+77delinsGA XP_011513575.1:n.2103+76_2103+77delinsGA
XM_011515274.1:c.1926+76_1926+77delinsGA XP_011513576.1:n.1926+76_1926+77delinsGA
XM_011515274.2:c.1926+76_1926+77delinsGA XP_011513576.1:n.1926+76_1926+77delinsGA
XM_017011997.1:c.2100+76_2100+77delinsGA XP_016867486.1:n.2100+76_2100+77delinsGA
NM_000168.6:c.2103+76_2103+77delinsGA MANE Select NP_000159.3:n.2103+76_2103+77delinsGA