Canonical Allele Identifier: CA454537646

Gene: GLI3

Linked Data

• MyVariant Identifiers: chr7:g.42088235T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42048636T>C , CM000669.2:g.42048636T>C	GRCh38
NC_000007.13:g.42088235T>C , CM000669.1:g.42088235T>C	GRCh37
NC_000007.12:g.42054760T>C	NCBI36
NG_008434.1:g.193384A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.534A>G MANE Select	ENSP00000379258.3:p.Pro178=
ENST00000677288.1:c.357A>G	ENSP00000503986.1:p.Pro119=
ENST00000677605.1:c.534A>G	ENSP00000503743.1:p.Pro178=
ENST00000678429.1:c.534A>G	ENSP00000502957.1:p.Pro178=
ENST00000395925.7:c.534A>G	ENSP00000379258.3:p.Pro178=
ENST00000448703.5:c.534A>G	ENSP00000406135.1:p.Pro178=
ENST00000479210.1:n.511A>G
NM_000168.5:c.534A>G	NP_000159.3:p.Pro178=
XM_005249703.1:c.534A>G	XP_005249760.1:p.Pro178=
XM_005249704.2:c.534A>G	XP_005249761.1:p.Pro178=
XM_011515272.1:c.534A>G	XP_011513574.1:p.Pro178=
XM_011515273.1:c.534A>G	XP_011513575.1:p.Pro178=
XM_011515274.1:c.357A>G	XP_011513576.1:p.Pro119=
XM_011515274.2:c.357A>G	XP_011513576.1:p.Pro119=
XM_017011997.1:c.531A>G	XP_016867486.1:p.Pro177=
NM_000168.6:c.534A>G MANE Select	NP_000159.3:p.Pro178=