Canonical Allele Identifier: CA367550151

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42076858C>G , CM000669.2:g.42076858C>G	GRCh38
NC_000007.13:g.42116457C>G , CM000669.1:g.42116457C>G	GRCh37
NC_000007.12:g.42082982C>G	NCBI36
NG_008434.1:g.165162G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000168.6:c.368-1G>C MANE Select	NP_000159.3:n.368-1G>C
ENST00000395925.8:c.368-1G>C MANE Select	ENSP00000379258.3:n.368-1G>C
NM_000168.5:c.368-1G>C	NP_000159.3:n.368-1G>C
ENST00000395925.7:c.368-1G>C	ENSP00000379258.3:n.368-1G>C
ENST00000448703.5:c.368-1G>C	ENSP00000406135.1:n.368-1G>C
ENST00000479210.1:n.345-1G>C
ENST00000677288.1:c.191-1G>C	ENSP00000503986.1:n.191-1G>C
ENST00000677605.1:c.368-1G>C	ENSP00000503743.1:n.368-1G>C
ENST00000678429.1:c.368-1G>C	ENSP00000502957.1:n.368-1G>C
XM_005249703.1:c.368-1G>C	XP_005249760.1:n.368-1G>C
XM_005249704.2:c.368-1G>C	XP_005249761.1:n.368-1G>C
XM_011515272.1:c.368-1G>C	XP_011513574.1:n.368-1G>C
XM_011515273.1:c.368-1G>C	XP_011513575.1:n.368-1G>C
XM_011515274.1:c.191-1G>C	XP_011513576.1:n.191-1G>C
XM_011515274.2:c.191-1G>C	XP_011513576.1:n.191-1G>C
XM_017011997.1:c.365-1G>C	XP_016867486.1:n.365-1G>C