Canonical Allele Identifier: CA1702731613

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42148135_42148161delinsGCACACACACACACACACACACACACA , CM000669.2:g.42148135_42148161delinsGCACACACACACACACACACACACACA	GRCh38
NC_000007.13:g.42187734_42187760delinsGCACACACACACACACACACACACACA , CM000669.1:g.42187734_42187760delinsGCACACACACACACACACACACACACA	GRCh37
NC_000007.12:g.42154259_42154285delinsGCACACACACACACACACACACACACA	NCBI36
NG_008434.1:g.93859_93885delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC MANE Select	ENSP00000379258.3:n.367+65_367+91delinsTG...
ENST00000642432.1:c.190+65_190+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000495498.1:n.190+65_190+91delinsTG...
ENST00000643264.1:c.190+65_190+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000495207.1:n.190+65_190+91delinsTG...
ENST00000647255.1:c.190+65_190+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000495745.1:n.190+65_190+91delinsTG...
ENST00000677288.1:c.190+65_190+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000503986.1:n.190+65_190+91delinsTG...
ENST00000677605.1:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000503743.1:n.367+65_367+91delinsTG...
ENST00000678429.1:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000502957.1:n.367+65_367+91delinsTG...
ENST00000395925.7:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000379258.3:n.367+65_367+91delinsTG...
ENST00000448703.5:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	ENSP00000406135.1:n.367+65_367+91delinsTG...
ENST00000479210.1:n.344+65_344+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC
NM_000168.5:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	NP_000159.3:n.367+65_367+91delinsTGTGTGTG...
XM_005249703.1:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	XP_005249760.1:n.367+65_367+91delinsTGTGT...
XM_005249704.2:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	XP_005249761.1:n.367+65_367+91delinsTGTGT...
XM_011515272.1:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	XP_011513574.1:n.367+65_367+91delinsTGTGT...
XM_011515273.1:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	XP_011513575.1:n.367+65_367+91delinsTGTGT...
XM_011515274.1:c.190+65_190+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	XP_011513576.1:n.190+65_190+91delinsTGTGT...
XM_011515274.2:c.190+65_190+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	XP_011513576.1:n.190+65_190+91delinsTGTGT...
XM_017011997.1:c.364+65_364+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC	XP_016867486.1:n.364+65_364+91delinsTGTGT...
NM_000168.6:c.367+65_367+91delinsTGTGTGTGTGTGTGTGTGTGTGTGTGC MANE Select	NP_000159.3:n.367+65_367+91delinsTGTGTGTG...