Canonical Allele Identifier: CA454525639

Gene: GLI3

Linked Data

• MyVariant Identifiers: chr7:g.42012041G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41972442G>C , CM000669.2:g.41972442G>C	GRCh38
NC_000007.13:g.42012041G>C , CM000669.1:g.42012041G>C	GRCh37
NC_000007.12:g.41978566G>C	NCBI36
NG_008434.1:g.269578C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.1998C>G MANE Select	ENSP00000379258.3:p.Gly666=
ENST00000677288.1:c.1824C>G	ENSP00000503986.1:p.Gly608=
ENST00000677605.1:c.1998C>G	ENSP00000503743.1:p.Gly666=
ENST00000678429.1:c.1998C>G	ENSP00000502957.1:p.Gly666=
ENST00000395925.7:c.1998C>G	ENSP00000379258.3:p.Gly666=
ENST00000464291.1:n.551C>G
ENST00000479210.1:n.1975C>G
NM_000168.5:c.1998C>G	NP_000159.3:p.Gly666=
XM_005249703.1:c.1998C>G	XP_005249760.1:p.Gly666=
XM_005249704.2:c.1998C>G	XP_005249761.1:p.Gly666=
XM_011515272.1:c.1998C>G	XP_011513574.1:p.Gly666=
XM_011515273.1:c.1998C>G	XP_011513575.1:p.Gly666=
XM_011515274.1:c.1821C>G	XP_011513576.1:p.Gly607=
XM_011515274.2:c.1821C>G	XP_011513576.1:p.Gly607=
XM_017011997.1:c.1995C>G	XP_016867486.1:p.Gly665=
NM_000168.6:c.1998C>G MANE Select	NP_000159.3:p.Gly666=