Canonical Allele Identifier: CA2038880594
Gene: GLI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57466094A= , CM000674.2:g.57466094A= GRCh38
NC_000012.11:g.57859877A= , CM000674.1:g.57859877A= GRCh37
NC_000012.10:g.56146144A= NCBI36
NG_029564.1:g.10960A=

Transcript Alleles

HGVS Amino-acid change
ENST00000228682.7:c.763-146A= MANE Select ENSP00000228682.2:n.763-146A=
ENST00000228682.6:c.763-146A= ENSP00000228682.2:n.763-146A=
ENST00000527742.1:n.629A=
ENST00000528467.1:c.640-146A= ENSP00000434408.1:n.640-146A=
ENST00000532291.5:c.379-146A= ENSP00000436671.1:n.379-146A=
ENST00000543426.5:c.379-146A= ENSP00000437607.1:n.379-146A=
ENST00000546141.5:c.640-146A= ENSP00000441006.1:n.640-146A=
NM_001160045.1:c.379-146A= NP_001153517.1:n.379-146A=
NM_001167609.1:c.640-146A= NP_001161081.1:n.640-146A=
NM_005269.2:c.763-146A= NP_005260.1:n.763-146A=
XM_005268799.2:c.379-146A= XP_005268856.1:n.379-146A=
XM_011538189.1:c.763-146A= XP_011536491.1:n.763-146A=
XM_011538190.1:c.763-146A= XP_011536492.1:n.763-146A=
XM_011538189.2:c.763-146A= XP_011536491.1:n.763-146A=
XM_011538190.2:c.763-146A= XP_011536492.1:n.763-146A=
NM_005269.3:c.763-146A= MANE Select NP_005260.1:n.763-146A=
NM_001160045.2:c.379-146A= NP_001153517.1:n.379-146A=
NM_001167609.2:c.640-146A= NP_001161081.1:n.640-146A=