Canonical Allele Identifier: CA1702661927

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41967794C= , CM000669.2:g.41967794C=	GRCh38
NC_000007.13:g.42007392C= , CM000669.1:g.42007392C=	GRCh37
NC_000007.12:g.41973917C=	NCBI36
NG_008434.1:g.274227G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.2233G= MANE Select	ENSP00000379258.3:p.Asp745=
ENST00000677288.1:c.2059G=	ENSP00000503986.1:p.Asp687=
ENST00000677605.1:c.2233G=	ENSP00000503743.1:p.Asp745=
ENST00000678429.1:c.2233G=	ENSP00000502957.1:p.Asp745=
ENST00000395925.7:c.2233G=	ENSP00000379258.3:p.Asp745=
ENST00000479210.1:n.2210G=
NM_000168.5:c.2233G=	NP_000159.3:p.Asp745=
XM_005249703.1:c.2233G=	XP_005249760.1:p.Asp745=
XM_005249704.2:c.2233G=	XP_005249761.1:p.Asp745=
XM_011515272.1:c.2233G=	XP_011513574.1:p.Asp745=
XM_011515273.1:c.2233G=	XP_011513575.1:p.Asp745=
XM_011515274.1:c.2056G=	XP_011513576.1:p.Asp686=
XM_011515274.2:c.2056G=	XP_011513576.1:p.Asp686=
XM_017011997.1:c.2230G=	XP_016867486.1:p.Asp744=
NM_000168.6:c.2233G= MANE Select	NP_000159.3:p.Asp745=