Canonical Allele Identifier: CA2573133168

Gene: GLI2

Linked Data

• ClinVar Variation Id: 1606596
• ClinVar RCV Id: RCV002152168
• dbSNP Id: rs2104965814

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120955445_120955446delinsTG , CM000664.2:g.120955445_120955446delinsTG	GRCh38
NC_000002.11:g.121713021_121713022delinsTG , CM000664.1:g.121713021_121713022delinsTG	GRCh37
NC_000002.10:g.121429491_121429492delinsTG	NCBI36
NG_009030.1:g.163155_163156delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.643+15_643+16delinsTG MANE Select	ENSP00000354586.5:n.643+15_643+16delinsTG
ENST00000452319.6:c.643+15_643+16delinsTG	ENSP00000390436.1:n.643+15_643+16delinsTG
ENST00000314490.15:c.-139-14948_-139-14947delinsTG	ENSP00000312694.12:n.-139-14948_-139-14947delinsTG
ENST00000341310.10:c.149-14948_149-14947delinsTG	ENSP00000344473.6:n.149-14948_149-14947delinsTG
ENST00000360874.10:c.231-13269_231-13268delinsTG	ENSP00000441454.1:n.231-13269_231-13268delinsTG
ENST00000361492.8:c.643+15_643+16delinsTG	ENSP00000354586.4:n.643+15_643+16delinsTG
ENST00000433812.1:c.513+15_513+16delinsTG	ENSP00000402383.1:n.513+15_513+16delinsTG
ENST00000435313.6:n.668+15_668+16delinsTG
ENST00000437950.5:c.149-14948_149-14947delinsTG	ENSP00000415773.1:n.149-14948_149-14947delinsTG
ENST00000438299.5:c.149-14948_149-14947delinsTG	ENSP00000400593.1:n.149-14948_149-14947delinsTG
ENST00000445186.5:c.149-14948_149-14947delinsTG	ENSP00000397488.1:n.149-14948_149-14947delinsTG
ENST00000452319.5:c.643+15_643+16delinsTG	ENSP00000390436.1:n.643+15_643+16delinsTG
ENST00000452692.5:c.149-14948_149-14947delinsTG	ENSP00000403715.1:n.149-14948_149-14947delinsTG
NM_005270.4:c.643+15_643+16delinsTG	NP_005261.2:n.643+15_643+16delinsTG
XM_006712422.1:c.643+15_643+16delinsTG	XP_006712485.1:n.643+15_643+16delinsTG
XM_011510969.1:c.625+15_625+16delinsTG	XP_011509271.1:n.625+15_625+16delinsTG
XM_011510970.1:c.502+15_502+16delinsTG	XP_011509272.1:n.502+15_502+16delinsTG
XM_011510971.1:c.448+15_448+16delinsTG	XP_011509273.1:n.448+15_448+16delinsTG
XM_011510972.1:c.448+15_448+16delinsTG	XP_011509274.1:n.448+15_448+16delinsTG
XM_011510973.1:c.268+15_268+16delinsTG	XP_011509275.1:n.268+15_268+16delinsTG
XM_011510974.1:c.268+15_268+16delinsTG	XP_011509276.1:n.268+15_268+16delinsTG
XM_006712422.3:c.643+15_643+16delinsTG	XP_006712485.1:n.643+15_643+16delinsTG
XM_011510969.2:c.895+15_895+16delinsTG	XP_011509271.2:n.895+15_895+16delinsTG
XM_011510970.2:c.502+15_502+16delinsTG	XP_011509272.1:n.502+15_502+16delinsTG
XM_011510971.2:c.448+15_448+16delinsTG	XP_011509273.1:n.448+15_448+16delinsTG
XM_011510972.2:c.544+15_544+16delinsTG	XP_011509274.2:n.544+15_544+16delinsTG
XM_011510973.2:c.268+15_268+16delinsTG	XP_011509275.1:n.268+15_268+16delinsTG
XM_011510974.2:c.268+15_268+16delinsTG	XP_011509276.1:n.268+15_268+16delinsTG
XM_017003818.1:c.895+15_895+16delinsTG	XP_016859307.1:n.895+15_895+16delinsTG
XM_024452794.1:c.643+15_643+16delinsTG	XP_024308562.1:n.643+15_643+16delinsTG
XM_024452795.1:c.643+15_643+16delinsTG	XP_024308563.1:n.643+15_643+16delinsTG
NM_001371271.1:c.643+15_643+16delinsTG	NP_001358200.1:n.643+15_643+16delinsTG
NM_001374353.1:c.643+15_643+16delinsTG MANE Select	NP_001361282.1:n.643+15_643+16delinsTG
NM_001374354.1:c.268+15_268+16delinsTG	NP_001361283.1:n.268+15_268+16delinsTG
NM_005270.5:c.643+15_643+16delinsTG	NP_005261.2:n.643+15_643+16delinsTG