Canonical Allele Identifier: CA454537622

Gene: GLI3

Linked Data

• MyVariant Identifiers: chr7:g.42088202G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42048603G>C , CM000669.2:g.42048603G>C	GRCh38
NC_000007.13:g.42088202G>C , CM000669.1:g.42088202G>C	GRCh37
NC_000007.12:g.42054727G>C	NCBI36
NG_008434.1:g.193417C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.567C>G MANE Select	ENSP00000379258.3:p.Pro189=
ENST00000677288.1:c.390C>G	ENSP00000503986.1:p.Pro130=
ENST00000677605.1:c.567C>G	ENSP00000503743.1:p.Pro189=
ENST00000678429.1:c.567C>G	ENSP00000502957.1:p.Pro189=
ENST00000395925.7:c.567C>G	ENSP00000379258.3:p.Pro189=
ENST00000479210.1:n.544C>G
NM_000168.5:c.567C>G	NP_000159.3:p.Pro189=
XM_005249703.1:c.567C>G	XP_005249760.1:p.Pro189=
XM_005249704.2:c.567C>G	XP_005249761.1:p.Pro189=
XM_011515272.1:c.567C>G	XP_011513574.1:p.Pro189=
XM_011515273.1:c.567C>G	XP_011513575.1:p.Pro189=
XM_011515274.1:c.390C>G	XP_011513576.1:p.Pro130=
XM_011515274.2:c.390C>G	XP_011513576.1:p.Pro130=
XM_017011997.1:c.564C>G	XP_016867486.1:p.Pro188=
NM_000168.6:c.567C>G MANE Select	NP_000159.3:p.Pro189=