Canonical Allele Identifier: CA1702660898

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965710_41965711delinsTT , CM000669.2:g.41965710_41965711delinsTT	GRCh38
NC_000007.13:g.42005308_42005309delinsTT , CM000669.1:g.42005308_42005309delinsTT	GRCh37
NC_000007.12:g.41971833_41971834delinsTT	NCBI36
NG_008434.1:g.276310_276311delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.3362_3363delinsAA MANE Select	ENSP00000379258.3:p.Lys1121=
ENST00000677288.1:c.3188_3189delinsAA	ENSP00000503986.1:p.Lys1063=
ENST00000677605.1:c.3362_3363delinsAA	ENSP00000503743.1:p.Lys1121=
ENST00000678429.1:c.3362_3363delinsAA	ENSP00000502957.1:p.Lys1121=
ENST00000395925.7:c.3362_3363delinsAA	ENSP00000379258.3:p.Lys1121=
ENST00000479210.1:n.3339_3340delinsAA
NM_000168.5:c.3362_3363delinsAA	NP_000159.3:p.Lys1121=
XM_005249703.1:c.3362_3363delinsAA	XP_005249760.1:p.Lys1121=
XM_005249704.2:c.3362_3363delinsAA	XP_005249761.1:p.Lys1121=
XM_011515272.1:c.3362_3363delinsAA	XP_011513574.1:p.Lys1121=
XM_011515273.1:c.3362_3363delinsAA	XP_011513575.1:p.Lys1121=
XM_011515274.1:c.3185_3186delinsAA	XP_011513576.1:p.Lys1062=
XM_011515274.2:c.3185_3186delinsAA	XP_011513576.1:p.Lys1062=
XM_017011997.1:c.3359_3360delinsAA	XP_016867486.1:p.Lys1120=
NM_000168.6:c.3362_3363delinsAA MANE Select	NP_000159.3:p.Lys1121=