Canonical Allele Identifier: CA1283795398

Gene: GLI2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120988987T= , CM000664.2:g.120988987T=	GRCh38
NC_000002.11:g.121746563T= , CM000664.1:g.121746563T=	GRCh37
NC_000002.10:g.121463033T=	NCBI36
NG_009030.1:g.196697T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.3022T= MANE Select	ENSP00000354586.5:p.Ser1008=
ENST00000452319.6:c.3073T=	ENSP00000390436.1:p.Ser1025=
ENST00000341310.10:c.*2121T=	ENSP00000344473.6:n.*2121T=
ENST00000361492.8:c.3073T=	ENSP00000354586.4:p.Ser1025=
ENST00000438299.5:c.*2172T=	ENSP00000400593.1:n.*2172T=
ENST00000445186.5:c.*2172T=	ENSP00000397488.1:n.*2172T=
ENST00000452319.5:c.3073T=	ENSP00000390436.1:p.Ser1025=
ENST00000452692.5:c.*2121T=	ENSP00000403715.1:n.*2121T=
NM_005270.4:c.3073T=	NP_005261.2:p.Ser1025=
XM_006712422.1:c.3022T=	XP_006712485.1:p.Ser1008=
XM_011510969.1:c.3055T=	XP_011509271.1:p.Ser1019=
XM_011510970.1:c.2932T=	XP_011509272.1:p.Ser978=
XM_011510971.1:c.2878T=	XP_011509273.1:p.Ser960=
XM_011510972.1:c.2878T=	XP_011509274.1:p.Ser960=
XM_011510973.1:c.2698T=	XP_011509275.1:p.Ser900=
XM_011510974.1:c.2647T=	XP_011509276.1:p.Ser883=
XM_006712422.3:c.3022T=	XP_006712485.1:p.Ser1008=
XM_011510969.2:c.3325T=	XP_011509271.2:p.Ser1109=
XM_011510970.2:c.2932T=	XP_011509272.1:p.Ser978=
XM_011510971.2:c.2878T=	XP_011509273.1:p.Ser960=
XM_011510972.2:c.2974T=	XP_011509274.2:p.Ser992=
XM_011510973.2:c.2698T=	XP_011509275.1:p.Ser900=
XM_011510974.2:c.2647T=	XP_011509276.1:p.Ser883=
XM_017003818.1:c.3274T=	XP_016859307.1:p.Ser1092=
XM_024452794.1:c.3073T=	XP_024308562.1:p.Ser1025=
XM_024452795.1:c.3073T=	XP_024308563.1:p.Ser1025=
NM_001371271.1:c.3073T=	NP_001358200.1:p.Ser1025=
NM_001374353.1:c.3022T= MANE Select	NP_001361282.1:p.Ser1008=
NM_001374354.1:c.2647T=	NP_001361283.1:p.Ser883=
NM_005270.5:c.3073T=	NP_005261.2:p.Ser1025=