Canonical Allele Identifier: CA428559483

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121748185C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120990609C>G , CM000664.2:g.120990609C>G	GRCh38
NC_000002.11:g.121748185C>G , CM000664.1:g.121748185C>G	GRCh37
NC_000002.10:g.121464655C>G	NCBI36
NG_009030.1:g.198319C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.4644C>G MANE Select	ENSP00000354586.5:p.Val1548=
ENST00000452319.6:c.4695C>G	ENSP00000390436.1:p.Val1565=
ENST00000341310.10:c.*3743C>G	ENSP00000344473.6:n.*3743C>G
ENST00000361492.8:c.4695C>G	ENSP00000354586.4:p.Val1565=
ENST00000438299.5:c.*2563C>G	ENSP00000400593.1:n.*2563C>G
ENST00000445186.5:c.*3794C>G	ENSP00000397488.1:n.*3794C>G
ENST00000452319.5:c.4695C>G	ENSP00000390436.1:p.Val1565=
ENST00000452692.5:c.*2512C>G	ENSP00000403715.1:n.*2512C>G
NM_005270.4:c.4695C>G	NP_005261.2:p.Val1565=
XM_006712422.1:c.4644C>G	XP_006712485.1:p.Val1548=
XM_011510969.1:c.4677C>G	XP_011509271.1:p.Val1559=
XM_011510970.1:c.4554C>G	XP_011509272.1:p.Val1518=
XM_011510971.1:c.4500C>G	XP_011509273.1:p.Val1500=
XM_011510972.1:c.4500C>G	XP_011509274.1:p.Val1500=
XM_011510973.1:c.4320C>G	XP_011509275.1:p.Val1440=
XM_011510974.1:c.4269C>G	XP_011509276.1:p.Val1423=
XM_006712422.3:c.4644C>G	XP_006712485.1:p.Val1548=
XM_011510969.2:c.4947C>G	XP_011509271.2:p.Val1649=
XM_011510970.2:c.4554C>G	XP_011509272.1:p.Val1518=
XM_011510971.2:c.4500C>G	XP_011509273.1:p.Val1500=
XM_011510972.2:c.4596C>G	XP_011509274.2:p.Val1532=
XM_011510973.2:c.4320C>G	XP_011509275.1:p.Val1440=
XM_011510974.2:c.4269C>G	XP_011509276.1:p.Val1423=
XM_017003818.1:c.4896C>G	XP_016859307.1:p.Val1632=
XM_024452794.1:c.4695C>G	XP_024308562.1:p.Val1565=
XM_024452795.1:c.4695C>G	XP_024308563.1:p.Val1565=
NM_001371271.1:c.4695C>G	NP_001358200.1:p.Val1565=
NM_001374353.1:c.4644C>G MANE Select	NP_001361282.1:p.Val1548=
NM_001374354.1:c.4269C>G	NP_001361283.1:p.Val1423=
NM_005270.5:c.4695C>G	NP_005261.2:p.Val1565=