Canonical Allele Identifier: CA2842944044

Gene: GLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57465974T>G , CM000674.2:g.57465974T>G	GRCh38
NC_000012.11:g.57859757T>G , CM000674.1:g.57859757T>G	GRCh37
NC_000012.10:g.56146024T>G	NCBI36
NG_029564.1:g.10840T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228682.7:c.762+49T>G MANE Select	ENSP00000228682.2:n.762+49T>G
ENST00000228682.6:c.762+49T>G	ENSP00000228682.2:n.762+49T>G
ENST00000527742.1:n.509T>G
ENST00000528467.1:c.639+49T>G	ENSP00000434408.1:n.639+49T>G
ENST00000532291.5:c.378+49T>G	ENSP00000436671.1:n.378+49T>G
ENST00000543426.5:c.378+49T>G	ENSP00000437607.1:n.378+49T>G
ENST00000546141.5:c.639+49T>G	ENSP00000441006.1:n.639+49T>G
NM_001160045.1:c.378+49T>G	NP_001153517.1:n.378+49T>G
NM_001167609.1:c.639+49T>G	NP_001161081.1:n.639+49T>G
NM_005269.2:c.762+49T>G	NP_005260.1:n.762+49T>G
XM_005268799.2:c.378+49T>G	XP_005268856.1:n.378+49T>G
XM_011538189.1:c.762+49T>G	XP_011536491.1:n.762+49T>G
XM_011538190.1:c.762+49T>G	XP_011536492.1:n.762+49T>G
XM_011538189.2:c.762+49T>G	XP_011536491.1:n.762+49T>G
XM_011538190.2:c.762+49T>G	XP_011536492.1:n.762+49T>G
NM_005269.3:c.762+49T>G MANE Select	NP_005260.1:n.762+49T>G
NM_001160045.2:c.378+49T>G	NP_001153517.1:n.378+49T>G
NM_001167609.2:c.639+49T>G	NP_001161081.1:n.639+49T>G