Canonical Allele Identifier: CA157305599

Gene: GLI3

Linked Data

• dbSNP Id: rs954024196
• MyVariant Identifiers: chr7:g.42276592G>A (hg19) ; chr7:g.42236993G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42236993G>A , CM000669.2:g.42236993G>A	GRCh38
NC_000007.13:g.42276592G>A , CM000669.1:g.42276592G>A	GRCh37
NC_000007.12:g.42243117G>A	NCBI36
NG_008434.1:g.5027C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.-65C>T MANE Select	ENSP00000379258.3:n.-65C>T
ENST00000428534.2:c.-43+791C>T	ENSP00000503957.1:n.-43+791C>T
ENST00000677605.1:c.-43+506C>T	ENSP00000503743.1:n.-43+506C>T
ENST00000677990.1:n.217C>T
ENST00000678978.1:c.-42-13698C>T	ENSP00000503352.1:n.-42-13698C>T
ENST00000395925.7:c.-65C>T	ENSP00000379258.3:n.-65C>T
ENST00000428534.1:n.87+791C>T
ENST00000437480.1:c.-65C>T	ENSP00000407963.1:n.-65C>T
NM_000168.5:c.-65C>T	NP_000159.3:n.-65C>T
XM_005249703.1:c.-43+791C>T	XP_005249760.1:n.-43+791C>T
XM_005249704.2:c.-43+506C>T	XP_005249761.1:n.-43+506C>T
XM_011515273.1:c.-42-13698C>T	XP_011513575.1:n.-42-13698C>T
NM_000168.6:c.-65C>T MANE Select	NP_000159.3:n.-65C>T