Canonical Allele Identifier: CA1702661045

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965988_41965989delinsTG , CM000669.2:g.41965988_41965989delinsTG	GRCh38
NC_000007.13:g.42005586_42005587delinsTG , CM000669.1:g.42005586_42005587delinsTG	GRCh37
NC_000007.12:g.41972111_41972112delinsTG	NCBI36
NG_008434.1:g.276032_276033delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.3084_3085delinsCA MANE Select	ENSP00000379258.3:p.Ser1028=
ENST00000677288.1:c.2910_2911delinsCA	ENSP00000503986.1:p.Ser970=
ENST00000677605.1:c.3084_3085delinsCA	ENSP00000503743.1:p.Ser1028=
ENST00000678429.1:c.3084_3085delinsCA	ENSP00000502957.1:p.Ser1028=
ENST00000395925.7:c.3084_3085delinsCA	ENSP00000379258.3:p.Ser1028=
ENST00000479210.1:n.3061_3062delinsCA
NM_000168.5:c.3084_3085delinsCA	NP_000159.3:p.Ser1028=
XM_005249703.1:c.3084_3085delinsCA	XP_005249760.1:p.Ser1028=
XM_005249704.2:c.3084_3085delinsCA	XP_005249761.1:p.Ser1028=
XM_011515272.1:c.3084_3085delinsCA	XP_011513574.1:p.Ser1028=
XM_011515273.1:c.3084_3085delinsCA	XP_011513575.1:p.Ser1028=
XM_011515274.1:c.2907_2908delinsCA	XP_011513576.1:p.Ser969=
XM_011515274.2:c.2907_2908delinsCA	XP_011513576.1:p.Ser969=
XM_017011997.1:c.3081_3082delinsCA	XP_016867486.1:p.Ser1027=
NM_000168.6:c.3084_3085delinsCA MANE Select	NP_000159.3:p.Ser1028=