Canonical Allele Identifier: CA348161677

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121736149A>C (hg19) ; chr2:g.120978573A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978573A>C , CM000664.2:g.120978573A>C	GRCh38
NC_000002.11:g.121736149A>C , CM000664.1:g.121736149A>C	GRCh37
NC_000002.10:g.121452619A>C	NCBI36
NG_009030.1:g.186283A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1457A>C MANE Select	ENSP00000354586.5:p.His486Pro
ENST00000452319.6:c.1508A>C	ENSP00000390436.1:p.His503Pro
ENST00000314490.15:c.521A>C	ENSP00000312694.12:p.His174Pro
ENST00000341310.10:c.*556A>C	ENSP00000344473.6:n.*556A>C
ENST00000361492.8:c.1508A>C	ENSP00000354586.4:p.His503Pro
ENST00000435313.6:n.1482A>C
ENST00000437950.5:c.*607A>C	ENSP00000415773.1:n.*607A>C
ENST00000438299.5:c.*607A>C	ENSP00000400593.1:n.*607A>C
ENST00000445186.5:c.*607A>C	ENSP00000397488.1:n.*607A>C
ENST00000452319.5:c.1508A>C	ENSP00000390436.1:p.His503Pro
ENST00000452692.5:c.*556A>C	ENSP00000403715.1:n.*556A>C
NM_005270.4:c.1508A>C	NP_005261.2:p.His503Pro
XM_006712422.1:c.1457A>C	XP_006712485.1:p.His486Pro
XM_011510969.1:c.1490A>C	XP_011509271.1:p.His497Pro
XM_011510970.1:c.1367A>C	XP_011509272.1:p.His456Pro
XM_011510971.1:c.1313A>C	XP_011509273.1:p.His438Pro
XM_011510972.1:c.1313A>C	XP_011509274.1:p.His438Pro
XM_011510973.1:c.1133A>C	XP_011509275.1:p.His378Pro
XM_011510974.1:c.1082A>C	XP_011509276.1:p.His361Pro
XM_006712422.3:c.1457A>C	XP_006712485.1:p.His486Pro
XM_011510969.2:c.1760A>C	XP_011509271.2:p.His587Pro
XM_011510970.2:c.1367A>C	XP_011509272.1:p.His456Pro
XM_011510971.2:c.1313A>C	XP_011509273.1:p.His438Pro
XM_011510972.2:c.1409A>C	XP_011509274.2:p.His470Pro
XM_011510973.2:c.1133A>C	XP_011509275.1:p.His378Pro
XM_011510974.2:c.1082A>C	XP_011509276.1:p.His361Pro
XM_017003818.1:c.1709A>C	XP_016859307.1:p.His570Pro
XM_024452794.1:c.1508A>C	XP_024308562.1:p.His503Pro
XM_024452795.1:c.1508A>C	XP_024308563.1:p.His503Pro
NM_001371271.1:c.1508A>C	NP_001358200.1:p.His503Pro
NM_001374353.1:c.1457A>C MANE Select	NP_001361282.1:p.His486Pro
NM_001374354.1:c.1082A>C	NP_001361283.1:p.His361Pro
NM_005270.5:c.1508A>C	NP_005261.2:p.His503Pro