Canonical Allele Identifier: CA1702661317

Gene: GLI3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41966458G= , CM000669.2:g.41966458G=	GRCh38
NC_000007.13:g.42006056G= , CM000669.1:g.42006056G=	GRCh37
NC_000007.12:g.41972581G=	NCBI36
NG_008434.1:g.275563C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395925.8:c.2615C= MANE Select	ENSP00000379258.3:p.Ser872=
ENST00000677288.1:c.2441C=	ENSP00000503986.1:p.Ser814=
ENST00000677605.1:c.2615C=	ENSP00000503743.1:p.Ser872=
ENST00000678429.1:c.2615C=	ENSP00000502957.1:p.Ser872=
ENST00000395925.7:c.2615C=	ENSP00000379258.3:p.Ser872=
ENST00000479210.1:n.2592C=
NM_000168.5:c.2615C=	NP_000159.3:p.Ser872=
XM_005249703.1:c.2615C=	XP_005249760.1:p.Ser872=
XM_005249704.2:c.2615C=	XP_005249761.1:p.Ser872=
XM_011515272.1:c.2615C=	XP_011513574.1:p.Ser872=
XM_011515273.1:c.2615C=	XP_011513575.1:p.Ser872=
XM_011515274.1:c.2438C=	XP_011513576.1:p.Ser813=
XM_011515274.2:c.2438C=	XP_011513576.1:p.Ser813=
XM_017011997.1:c.2612C=	XP_016867486.1:p.Ser871=
NM_000168.6:c.2615C= MANE Select	NP_000159.3:p.Ser872=