Canonical Allele Identifier: CA2562380379

Gene: GLI3

Linked Data

• gnomAD v4: 7-41961653-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41961653C>A , CM000669.2:g.41961653C>A	GRCh38
NC_000007.13:g.42001251C>A , CM000669.1:g.42001251C>A	GRCh37
NC_000007.12:g.41967776C>A	NCBI36
NG_008434.1:g.280368G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*2677G>T MANE Select	ENSP00000379258.3:n.*2677G>T
ENST00000677288.1:c.*2677G>T	ENSP00000503986.1:n.*2677G>T
ENST00000677605.1:c.*2677G>T	ENSP00000503743.1:n.*2677G>T
ENST00000678429.1:c.*2677G>T	ENSP00000502957.1:n.*2677G>T
ENST00000395925.7:c.*2677G>T	ENSP00000379258.3:n.*2677G>T
NM_000168.5:c.*2677G>T	NP_000159.3:n.*2677G>T
XM_005249703.1:c.*2677G>T	XP_005249760.1:n.*2677G>T
XM_005249704.2:c.*2677G>T	XP_005249761.1:n.*2677G>T
XM_011515272.1:c.*2677G>T	XP_011513574.1:n.*2677G>T
XM_011515273.1:c.*2677G>T	XP_011513575.1:n.*2677G>T
XM_011515274.1:c.*2677G>T	XP_011513576.1:n.*2677G>T
NM_000168.6:c.*2677G>T MANE Select	NP_000159.3:n.*2677G>T