Canonical Allele Identifier: CA348170971

Gene: GLI2

Linked Data

• gnomAD v4: 2-120988966-G-T
• MyVariant Identifiers: chr2:g.121746542G>T (hg19) ; chr2:g.120988966G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120988966G>T , CM000664.2:g.120988966G>T	GRCh38
NC_000002.11:g.121746542G>T , CM000664.1:g.121746542G>T	GRCh37
NC_000002.10:g.121463012G>T	NCBI36
NG_009030.1:g.196676G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.3001G>T MANE Select	ENSP00000354586.5:p.Gly1001Cys
ENST00000452319.6:c.3052G>T	ENSP00000390436.1:p.Gly1018Cys
ENST00000341310.10:c.*2100G>T	ENSP00000344473.6:n.*2100G>T
ENST00000361492.8:c.3052G>T	ENSP00000354586.4:p.Gly1018Cys
ENST00000438299.5:c.*2151G>T	ENSP00000400593.1:n.*2151G>T
ENST00000445186.5:c.*2151G>T	ENSP00000397488.1:n.*2151G>T
ENST00000452319.5:c.3052G>T	ENSP00000390436.1:p.Gly1018Cys
ENST00000452692.5:c.*2100G>T	ENSP00000403715.1:n.*2100G>T
NM_005270.4:c.3052G>T	NP_005261.2:p.Gly1018Cys
XM_006712422.1:c.3001G>T	XP_006712485.1:p.Gly1001Cys
XM_011510969.1:c.3034G>T	XP_011509271.1:p.Gly1012Cys
XM_011510970.1:c.2911G>T	XP_011509272.1:p.Gly971Cys
XM_011510971.1:c.2857G>T	XP_011509273.1:p.Gly953Cys
XM_011510972.1:c.2857G>T	XP_011509274.1:p.Gly953Cys
XM_011510973.1:c.2677G>T	XP_011509275.1:p.Gly893Cys
XM_011510974.1:c.2626G>T	XP_011509276.1:p.Gly876Cys
XM_006712422.3:c.3001G>T	XP_006712485.1:p.Gly1001Cys
XM_011510969.2:c.3304G>T	XP_011509271.2:p.Gly1102Cys
XM_011510970.2:c.2911G>T	XP_011509272.1:p.Gly971Cys
XM_011510971.2:c.2857G>T	XP_011509273.1:p.Gly953Cys
XM_011510972.2:c.2953G>T	XP_011509274.2:p.Gly985Cys
XM_011510973.2:c.2677G>T	XP_011509275.1:p.Gly893Cys
XM_011510974.2:c.2626G>T	XP_011509276.1:p.Gly876Cys
XM_017003818.1:c.3253G>T	XP_016859307.1:p.Gly1085Cys
XM_024452794.1:c.3052G>T	XP_024308562.1:p.Gly1018Cys
XM_024452795.1:c.3052G>T	XP_024308563.1:p.Gly1018Cys
NM_001371271.1:c.3052G>T	NP_001358200.1:p.Gly1018Cys
NM_001374353.1:c.3001G>T MANE Select	NP_001361282.1:p.Gly1001Cys
NM_001374354.1:c.2626G>T	NP_001361283.1:p.Gly876Cys
NM_005270.5:c.3052G>T	NP_005261.2:p.Gly1018Cys