Canonical Allele Identifier: CA1283796155

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990515T= , CM000664.2:g.120990515T=	GRCh38
NC_000002.11:g.121748091T= , CM000664.1:g.121748091T=	GRCh37
NC_000002.10:g.121464561T=	NCBI36
NG_009030.1:g.198225T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4550T= MANE Select	ENSP00000354586.5:p.Leu1517=
ENST00000452319.6:c.4601T=	ENSP00000390436.1:p.Leu1534=
ENST00000341310.10:c.*3649T=	ENSP00000344473.6:n.*3649T=
ENST00000361492.8:c.4601T=	ENSP00000354586.4:p.Leu1534=
ENST00000438299.5:c.*2544-75T=	ENSP00000400593.1:n.*2544-75T=
ENST00000445186.5:c.*3700T=	ENSP00000397488.1:n.*3700T=
ENST00000452319.5:c.4601T=	ENSP00000390436.1:p.Leu1534=
ENST00000452692.5:c.*2493-75T=	ENSP00000403715.1:n.*2493-75T=
NM_005270.4:c.4601T=	NP_005261.2:p.Leu1534=
XM_006712422.1:c.4550T=	XP_006712485.1:p.Leu1517=
XM_011510969.1:c.4583T=	XP_011509271.1:p.Leu1528=
XM_011510970.1:c.4460T=	XP_011509272.1:p.Leu1487=
XM_011510971.1:c.4406T=	XP_011509273.1:p.Leu1469=
XM_011510972.1:c.4406T=	XP_011509274.1:p.Leu1469=
XM_011510973.1:c.4226T=	XP_011509275.1:p.Leu1409=
XM_011510974.1:c.4175T=	XP_011509276.1:p.Leu1392=
XM_006712422.3:c.4550T=	XP_006712485.1:p.Leu1517=
XM_011510969.2:c.4853T=	XP_011509271.2:p.Leu1618=
XM_011510970.2:c.4460T=	XP_011509272.1:p.Leu1487=
XM_011510971.2:c.4406T=	XP_011509273.1:p.Leu1469=
XM_011510972.2:c.4502T=	XP_011509274.2:p.Leu1501=
XM_011510973.2:c.4226T=	XP_011509275.1:p.Leu1409=
XM_011510974.2:c.4175T=	XP_011509276.1:p.Leu1392=
XM_017003818.1:c.4802T=	XP_016859307.1:p.Leu1601=
XM_024452794.1:c.4601T=	XP_024308562.1:p.Leu1534=
XM_024452795.1:c.4601T=	XP_024308563.1:p.Leu1534=
NM_001371271.1:c.4601T=	NP_001358200.1:p.Leu1534=
NM_001374353.1:c.4550T= MANE Select	NP_001361282.1:p.Leu1517=
NM_001374354.1:c.4175T=	NP_001361283.1:p.Leu1392=
NM_005270.5:c.4601T=	NP_005261.2:p.Leu1534=