Canonical Allele Identifier: CA454537636

Gene: GLI3

Linked Data

• MyVariant Identifiers: chr7:g.42088220A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42048621A>G , CM000669.2:g.42048621A>G	GRCh38
NC_000007.13:g.42088220A>G , CM000669.1:g.42088220A>G	GRCh37
NC_000007.12:g.42054745A>G	NCBI36
NG_008434.1:g.193399T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.549T>C MANE Select	ENSP00000379258.3:p.Thr183=
ENST00000677288.1:c.372T>C	ENSP00000503986.1:p.Thr124=
ENST00000677605.1:c.549T>C	ENSP00000503743.1:p.Thr183=
ENST00000678429.1:c.549T>C	ENSP00000502957.1:p.Thr183=
ENST00000395925.7:c.549T>C	ENSP00000379258.3:p.Thr183=
ENST00000479210.1:n.526T>C
NM_000168.5:c.549T>C	NP_000159.3:p.Thr183=
XM_005249703.1:c.549T>C	XP_005249760.1:p.Thr183=
XM_005249704.2:c.549T>C	XP_005249761.1:p.Thr183=
XM_011515272.1:c.549T>C	XP_011513574.1:p.Thr183=
XM_011515273.1:c.549T>C	XP_011513575.1:p.Thr183=
XM_011515274.1:c.372T>C	XP_011513576.1:p.Thr124=
XM_011515274.2:c.372T>C	XP_011513576.1:p.Thr124=
XM_017011997.1:c.546T>C	XP_016867486.1:p.Thr182=
NM_000168.6:c.549T>C MANE Select	NP_000159.3:p.Thr183=