Canonical Allele Identifier: CA1702691540

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42040290C= , CM000669.2:g.42040290C=	GRCh38
NC_000007.13:g.42079889C= , CM000669.1:g.42079889C=	GRCh37
NC_000007.12:g.42046414C=	NCBI36
NG_008434.1:g.201730G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.827-51G= MANE Select	ENSP00000379258.3:n.827-51G=
ENST00000677288.1:c.650-51G=	ENSP00000503986.1:n.650-51G=
ENST00000677605.1:c.827-51G=	ENSP00000503743.1:n.827-51G=
ENST00000678429.1:c.827-51G=	ENSP00000502957.1:n.827-51G=
ENST00000395925.7:c.827-51G=	ENSP00000379258.3:n.827-51G=
ENST00000479210.1:n.804-51G=
NM_000168.5:c.827-51G=	NP_000159.3:n.827-51G=
XM_005249703.1:c.827-51G=	XP_005249760.1:n.827-51G=
XM_005249704.2:c.827-51G=	XP_005249761.1:n.827-51G=
XM_011515272.1:c.827-51G=	XP_011513574.1:n.827-51G=
XM_011515273.1:c.827-51G=	XP_011513575.1:n.827-51G=
XM_011515274.1:c.650-51G=	XP_011513576.1:n.650-51G=
XM_011515274.2:c.650-51G=	XP_011513576.1:n.650-51G=
XM_017011997.1:c.824-51G=	XP_016867486.1:n.824-51G=
NM_000168.6:c.827-51G= MANE Select	NP_000159.3:n.827-51G=