Canonical Allele Identifier: CA2682480055

Gene: GLI3

Linked Data

• gnomAD v4: 7-41961692-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41961692A>T , CM000669.2:g.41961692A>T	GRCh38
NC_000007.13:g.42001290A>T , CM000669.1:g.42001290A>T	GRCh37
NC_000007.12:g.41967815A>T	NCBI36
NG_008434.1:g.280329T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.*2638T>A MANE Select	ENSP00000379258.3:n.*2638T>A
ENST00000677288.1:c.*2638T>A	ENSP00000503986.1:n.*2638T>A
ENST00000677605.1:c.*2638T>A	ENSP00000503743.1:n.*2638T>A
ENST00000678429.1:c.*2638T>A	ENSP00000502957.1:n.*2638T>A
ENST00000395925.7:c.*2638T>A	ENSP00000379258.3:n.*2638T>A
NM_000168.5:c.*2638T>A	NP_000159.3:n.*2638T>A
XM_005249703.1:c.*2638T>A	XP_005249760.1:n.*2638T>A
XM_005249704.2:c.*2638T>A	XP_005249761.1:n.*2638T>A
XM_011515272.1:c.*2638T>A	XP_011513574.1:n.*2638T>A
XM_011515273.1:c.*2638T>A	XP_011513575.1:n.*2638T>A
XM_011515274.1:c.*2638T>A	XP_011513576.1:n.*2638T>A
NM_000168.6:c.*2638T>A MANE Select	NP_000159.3:n.*2638T>A