Canonical Allele Identifier: CA348180477
Gene: GLI2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120990662A>T , CM000664.2:g.120990662A>T GRCh38
NC_000002.11:g.121748238A>T , CM000664.1:g.121748238A>T GRCh37
NC_000002.10:g.121464708A>T NCBI36
NG_009030.1:g.198372A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361492.9:c.4697A>T MANE Select ENSP00000354586.5:p.Asn1566Ile
ENST00000452319.6:c.4748A>T ENSP00000390436.1:p.Asn1583Ile
ENST00000341310.10:c.*3796A>T ENSP00000344473.6:n.*3796A>T
ENST00000361492.8:c.4748A>T ENSP00000354586.4:p.Asn1583Ile
ENST00000438299.5:c.*2616A>T ENSP00000400593.1:n.*2616A>T
ENST00000445186.5:c.*3847A>T ENSP00000397488.1:n.*3847A>T
ENST00000452319.5:c.4748A>T ENSP00000390436.1:p.Asn1583Ile
ENST00000452692.5:c.*2565A>T ENSP00000403715.1:n.*2565A>T
NM_005270.4:c.4748A>T NP_005261.2:p.Asn1583Ile
XM_006712422.1:c.4697A>T XP_006712485.1:p.Asn1566Ile
XM_011510969.1:c.4730A>T XP_011509271.1:p.Asn1577Ile
XM_011510970.1:c.4607A>T XP_011509272.1:p.Asn1536Ile
XM_011510971.1:c.4553A>T XP_011509273.1:p.Asn1518Ile
XM_011510972.1:c.4553A>T XP_011509274.1:p.Asn1518Ile
XM_011510973.1:c.4373A>T XP_011509275.1:p.Asn1458Ile
XM_011510974.1:c.4322A>T XP_011509276.1:p.Asn1441Ile
XM_006712422.3:c.4697A>T XP_006712485.1:p.Asn1566Ile
XM_011510969.2:c.5000A>T XP_011509271.2:p.Asn1667Ile
XM_011510970.2:c.4607A>T XP_011509272.1:p.Asn1536Ile
XM_011510971.2:c.4553A>T XP_011509273.1:p.Asn1518Ile
XM_011510972.2:c.4649A>T XP_011509274.2:p.Asn1550Ile
XM_011510973.2:c.4373A>T XP_011509275.1:p.Asn1458Ile
XM_011510974.2:c.4322A>T XP_011509276.1:p.Asn1441Ile
XM_017003818.1:c.4949A>T XP_016859307.1:p.Asn1650Ile
XM_024452794.1:c.4748A>T XP_024308562.1:p.Asn1583Ile
XM_024452795.1:c.4748A>T XP_024308563.1:p.Asn1583Ile
NM_001371271.1:c.4748A>T NP_001358200.1:p.Asn1583Ile
NM_001374353.1:c.4697A>T MANE Select NP_001361282.1:p.Asn1566Ile
NM_001374354.1:c.4322A>T NP_001361283.1:p.Asn1441Ile
NM_005270.5:c.4748A>T NP_005261.2:p.Asn1583Ile