Canonical Allele Identifier: CA367323859

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42023505C>G , CM000669.2:g.42023505C>G	GRCh38
NC_000007.13:g.42063104C>G , CM000669.1:g.42063104C>G	GRCh37
NC_000007.12:g.42029629C>G	NCBI36
NG_008434.1:g.218515G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000168.6:c.1460G>C MANE Select	NP_000159.3:p.Cys487Ser
ENST00000395925.8:c.1460G>C MANE Select	ENSP00000379258.3:p.Cys487Ser
NM_000168.5:c.1460G>C	NP_000159.3:p.Cys487Ser
ENST00000395925.7:c.1460G>C	ENSP00000379258.3:p.Cys487Ser
ENST00000479210.1:n.1437G>C
ENST00000677288.1:c.1286G>C	ENSP00000503986.1:p.Cys429Ser
ENST00000677605.1:c.1460G>C	ENSP00000503743.1:p.Cys487Ser
ENST00000678429.1:c.1460G>C	ENSP00000502957.1:p.Cys487Ser
XM_005249703.1:c.1460G>C	XP_005249760.1:p.Cys487Ser
XM_005249704.2:c.1460G>C	XP_005249761.1:p.Cys487Ser
XM_011515272.1:c.1460G>C	XP_011513574.1:p.Cys487Ser
XM_011515273.1:c.1460G>C	XP_011513575.1:p.Cys487Ser
XM_011515274.1:c.1283G>C	XP_011513576.1:p.Cys428Ser
XM_011515274.2:c.1283G>C	XP_011513576.1:p.Cys428Ser
XM_017011997.1:c.1457G>C	XP_016867486.1:p.Cys486Ser