Canonical Allele Identifier: CA2682510063

Gene: GLI3

Linked Data

• gnomAD v4: 7-41965507-CGAGTCTGCGGCACAGCGGGCCGCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41965509_41965532del , CM000669.2:g.41965509_41965532del	GRCh38
NC_000007.13:g.42005107_42005130del , CM000669.1:g.42005107_42005130del	GRCh37
NC_000007.12:g.41971632_41971655del	NCBI36
NG_008434.1:g.276490_276513del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.3542_3565del MANE Select	ENSP00000379258.3:p.Pro1181_Thr1188del
ENST00000677288.1:c.3368_3391del	ENSP00000503986.1:p.Pro1123_Thr1130del
ENST00000677605.1:c.3542_3565del	ENSP00000503743.1:p.Pro1181_Thr1188del
ENST00000678429.1:c.3542_3565del	ENSP00000502957.1:p.Pro1181_Thr1188del
ENST00000395925.7:c.3542_3565del	ENSP00000379258.3:p.Pro1181_Thr1188del
ENST00000479210.1:n.3519_3542del
NM_000168.5:c.3542_3565del	NP_000159.3:p.Pro1181_Thr1188del
XM_005249703.1:c.3542_3565del	XP_005249760.1:p.Pro1181_Thr1188del
XM_005249704.2:c.3542_3565del	XP_005249761.1:p.Pro1181_Thr1188del
XM_011515272.1:c.3542_3565del	XP_011513574.1:p.Pro1181_Thr1188del
XM_011515273.1:c.3542_3565del	XP_011513575.1:p.Pro1181_Thr1188del
XM_011515274.1:c.3365_3388del	XP_011513576.1:p.Pro1122_Thr1129del
XM_011515274.2:c.3365_3388del	XP_011513576.1:p.Pro1122_Thr1129del
XM_017011997.1:c.3539_3562del	XP_016867486.1:p.Pro1180_Thr1187del
NM_000168.6:c.3542_3565del MANE Select	NP_000159.3:p.Pro1181_Thr1188del