Canonical Allele Identifier: CA1702690998

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040034A= , CM000669.2:g.42040034A=	GRCh38
NC_000007.13:g.42079633A= , CM000669.1:g.42079633A=	GRCh37
NC_000007.12:g.42046158A=	NCBI36
NG_008434.1:g.201986T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.1028+4T= MANE Select	ENSP00000379258.3:n.1028+4T=
ENST00000677288.1:c.851+4T=	ENSP00000503986.1:n.851+4T=
ENST00000677605.1:c.1028+4T=	ENSP00000503743.1:n.1028+4T=
ENST00000678429.1:c.1028+4T=	ENSP00000502957.1:n.1028+4T=
ENST00000395925.7:c.1028+4T=	ENSP00000379258.3:n.1028+4T=
ENST00000479210.1:n.1005+4T=
NM_000168.5:c.1028+4T=	NP_000159.3:n.1028+4T=
XM_005249703.1:c.1028+4T=	XP_005249760.1:n.1028+4T=
XM_005249704.2:c.1028+4T=	XP_005249761.1:n.1028+4T=
XM_011515272.1:c.1028+4T=	XP_011513574.1:n.1028+4T=
XM_011515273.1:c.1028+4T=	XP_011513575.1:n.1028+4T=
XM_011515274.1:c.851+4T=	XP_011513576.1:n.851+4T=
XM_011515274.2:c.851+4T=	XP_011513576.1:n.851+4T=
XM_017011997.1:c.1025+4T=	XP_016867486.1:n.1025+4T=
NM_000168.6:c.1028+4T= MANE Select	NP_000159.3:n.1028+4T=