Canonical Allele Identifier: CA348180072
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990511C>A , CM000664.2:g.120990511C>A GRCh38
NC_000002.11:g.121748087C>A , CM000664.1:g.121748087C>A GRCh37
NC_000002.10:g.121464557C>A NCBI36
NG_009030.1:g.198221C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4546C>A MANE Select ENSP00000354586.5:p.Leu1516Ile
ENST00000452319.6:c.4597C>A ENSP00000390436.1:p.Leu1533Ile
ENST00000341310.10:c.*3645C>A ENSP00000344473.6:n.*3645C>A
ENST00000361492.8:c.4597C>A ENSP00000354586.4:p.Leu1533Ile
ENST00000438299.5:c.*2544-79C>A ENSP00000400593.1:n.*2544-79C>A
ENST00000445186.5:c.*3696C>A ENSP00000397488.1:n.*3696C>A
ENST00000452319.5:c.4597C>A ENSP00000390436.1:p.Leu1533Ile
ENST00000452692.5:c.*2493-79C>A ENSP00000403715.1:n.*2493-79C>A
NM_005270.4:c.4597C>A NP_005261.2:p.Leu1533Ile
XM_006712422.1:c.4546C>A XP_006712485.1:p.Leu1516Ile
XM_011510969.1:c.4579C>A XP_011509271.1:p.Leu1527Ile
XM_011510970.1:c.4456C>A XP_011509272.1:p.Leu1486Ile
XM_011510971.1:c.4402C>A XP_011509273.1:p.Leu1468Ile
XM_011510972.1:c.4402C>A XP_011509274.1:p.Leu1468Ile
XM_011510973.1:c.4222C>A XP_011509275.1:p.Leu1408Ile
XM_011510974.1:c.4171C>A XP_011509276.1:p.Leu1391Ile
XM_006712422.3:c.4546C>A XP_006712485.1:p.Leu1516Ile
XM_011510969.2:c.4849C>A XP_011509271.2:p.Leu1617Ile
XM_011510970.2:c.4456C>A XP_011509272.1:p.Leu1486Ile
XM_011510971.2:c.4402C>A XP_011509273.1:p.Leu1468Ile
XM_011510972.2:c.4498C>A XP_011509274.2:p.Leu1500Ile
XM_011510973.2:c.4222C>A XP_011509275.1:p.Leu1408Ile
XM_011510974.2:c.4171C>A XP_011509276.1:p.Leu1391Ile
XM_017003818.1:c.4798C>A XP_016859307.1:p.Leu1600Ile
XM_024452794.1:c.4597C>A XP_024308562.1:p.Leu1533Ile
XM_024452795.1:c.4597C>A XP_024308563.1:p.Leu1533Ile
NM_001371271.1:c.4597C>A NP_001358200.1:p.Leu1533Ile
NM_001374353.1:c.4546C>A MANE Select NP_001361282.1:p.Leu1516Ile
NM_001374354.1:c.4171C>A NP_001361283.1:p.Leu1391Ile
NM_005270.5:c.4597C>A NP_005261.2:p.Leu1533Ile