Canonical Allele Identifier: CA428559478

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121748176C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990600C>T , CM000664.2:g.120990600C>T	GRCh38
NC_000002.11:g.121748176C>T , CM000664.1:g.121748176C>T	GRCh37
NC_000002.10:g.121464646C>T	NCBI36
NG_009030.1:g.198310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4635C>T MANE Select	ENSP00000354586.5:p.Asn1545=
ENST00000452319.6:c.4686C>T	ENSP00000390436.1:p.Asn1562=
ENST00000341310.10:c.*3734C>T	ENSP00000344473.6:n.*3734C>T
ENST00000361492.8:c.4686C>T	ENSP00000354586.4:p.Asn1562=
ENST00000438299.5:c.*2554C>T	ENSP00000400593.1:n.*2554C>T
ENST00000445186.5:c.*3785C>T	ENSP00000397488.1:n.*3785C>T
ENST00000452319.5:c.4686C>T	ENSP00000390436.1:p.Asn1562=
ENST00000452692.5:c.*2503C>T	ENSP00000403715.1:n.*2503C>T
NM_005270.4:c.4686C>T	NP_005261.2:p.Asn1562=
XM_006712422.1:c.4635C>T	XP_006712485.1:p.Asn1545=
XM_011510969.1:c.4668C>T	XP_011509271.1:p.Asn1556=
XM_011510970.1:c.4545C>T	XP_011509272.1:p.Asn1515=
XM_011510971.1:c.4491C>T	XP_011509273.1:p.Asn1497=
XM_011510972.1:c.4491C>T	XP_011509274.1:p.Asn1497=
XM_011510973.1:c.4311C>T	XP_011509275.1:p.Asn1437=
XM_011510974.1:c.4260C>T	XP_011509276.1:p.Asn1420=
XM_006712422.3:c.4635C>T	XP_006712485.1:p.Asn1545=
XM_011510969.2:c.4938C>T	XP_011509271.2:p.Asn1646=
XM_011510970.2:c.4545C>T	XP_011509272.1:p.Asn1515=
XM_011510971.2:c.4491C>T	XP_011509273.1:p.Asn1497=
XM_011510972.2:c.4587C>T	XP_011509274.2:p.Asn1529=
XM_011510973.2:c.4311C>T	XP_011509275.1:p.Asn1437=
XM_011510974.2:c.4260C>T	XP_011509276.1:p.Asn1420=
XM_017003818.1:c.4887C>T	XP_016859307.1:p.Asn1629=
XM_024452794.1:c.4686C>T	XP_024308562.1:p.Asn1562=
XM_024452795.1:c.4686C>T	XP_024308563.1:p.Asn1562=
NM_001371271.1:c.4686C>T	NP_001358200.1:p.Asn1562=
NM_001374353.1:c.4635C>T MANE Select	NP_001361282.1:p.Asn1545=
NM_001374354.1:c.4260C>T	NP_001361283.1:p.Asn1420=
NM_005270.5:c.4686C>T	NP_005261.2:p.Asn1562=