Canonical Allele Identifier: CA1702661237

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41966317_41966326delinsAGCAGGCTGG , CM000669.2:g.41966317_41966326delinsAGCAGGCTGG	GRCh38
NC_000007.13:g.42005915_42005924delinsAGCAGGCTGG , CM000669.1:g.42005915_42005924delinsAGCAGGCTGG	GRCh37
NC_000007.12:g.41972440_41972449delinsAGCAGGCTGG	NCBI36
NG_008434.1:g.275695_275704delinsCCAGCCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.2747_2756delinsCCAGCCTGCT MANE Select	ENSP00000379258.3:p.Pro916=
ENST00000677288.1:c.2573_2582delinsCCAGCCTGCT	ENSP00000503986.1:p.Pro858=
ENST00000677605.1:c.2747_2756delinsCCAGCCTGCT	ENSP00000503743.1:p.Pro916=
ENST00000678429.1:c.2747_2756delinsCCAGCCTGCT	ENSP00000502957.1:p.Pro916=
ENST00000395925.7:c.2747_2756delinsCCAGCCTGCT	ENSP00000379258.3:p.Pro916=
ENST00000479210.1:n.2724_2733delinsCCAGCCTGCT
NM_000168.5:c.2747_2756delinsCCAGCCTGCT	NP_000159.3:p.Pro916=
XM_005249703.1:c.2747_2756delinsCCAGCCTGCT	XP_005249760.1:p.Pro916=
XM_005249704.2:c.2747_2756delinsCCAGCCTGCT	XP_005249761.1:p.Pro916=
XM_011515272.1:c.2747_2756delinsCCAGCCTGCT	XP_011513574.1:p.Pro916=
XM_011515273.1:c.2747_2756delinsCCAGCCTGCT	XP_011513575.1:p.Pro916=
XM_011515274.1:c.2570_2579delinsCCAGCCTGCT	XP_011513576.1:p.Pro857=
XM_011515274.2:c.2570_2579delinsCCAGCCTGCT	XP_011513576.1:p.Pro857=
XM_017011997.1:c.2744_2753delinsCCAGCCTGCT	XP_016867486.1:p.Pro915=
NM_000168.6:c.2747_2756delinsCCAGCCTGCT MANE Select	NP_000159.3:p.Pro916=