Canonical Allele Identifier: CA348161670

Gene: GLI2

Linked Data

• MyVariant Identifiers: chr2:g.121736145C>T (hg19) ; chr2:g.120978569C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120978569C>T , CM000664.2:g.120978569C>T	GRCh38
NC_000002.11:g.121736145C>T , CM000664.1:g.121736145C>T	GRCh37
NC_000002.10:g.121452615C>T	NCBI36
NG_009030.1:g.186279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361492.9:c.1453C>T MANE Select	ENSP00000354586.5:p.Pro485Ser
ENST00000452319.6:c.1504C>T	ENSP00000390436.1:p.Pro502Ser
ENST00000314490.15:c.517C>T	ENSP00000312694.12:p.Pro173Ser
ENST00000341310.10:c.*552C>T	ENSP00000344473.6:n.*552C>T
ENST00000361492.8:c.1504C>T	ENSP00000354586.4:p.Pro502Ser
ENST00000435313.6:n.1478C>T
ENST00000437950.5:c.*603C>T	ENSP00000415773.1:n.*603C>T
ENST00000438299.5:c.*603C>T	ENSP00000400593.1:n.*603C>T
ENST00000445186.5:c.*603C>T	ENSP00000397488.1:n.*603C>T
ENST00000452319.5:c.1504C>T	ENSP00000390436.1:p.Pro502Ser
ENST00000452692.5:c.*552C>T	ENSP00000403715.1:n.*552C>T
NM_005270.4:c.1504C>T	NP_005261.2:p.Pro502Ser
XM_006712422.1:c.1453C>T	XP_006712485.1:p.Pro485Ser
XM_011510969.1:c.1486C>T	XP_011509271.1:p.Pro496Ser
XM_011510970.1:c.1363C>T	XP_011509272.1:p.Pro455Ser
XM_011510971.1:c.1309C>T	XP_011509273.1:p.Pro437Ser
XM_011510972.1:c.1309C>T	XP_011509274.1:p.Pro437Ser
XM_011510973.1:c.1129C>T	XP_011509275.1:p.Pro377Ser
XM_011510974.1:c.1078C>T	XP_011509276.1:p.Pro360Ser
XM_006712422.3:c.1453C>T	XP_006712485.1:p.Pro485Ser
XM_011510969.2:c.1756C>T	XP_011509271.2:p.Pro586Ser
XM_011510970.2:c.1363C>T	XP_011509272.1:p.Pro455Ser
XM_011510971.2:c.1309C>T	XP_011509273.1:p.Pro437Ser
XM_011510972.2:c.1405C>T	XP_011509274.2:p.Pro469Ser
XM_011510973.2:c.1129C>T	XP_011509275.1:p.Pro377Ser
XM_011510974.2:c.1078C>T	XP_011509276.1:p.Pro360Ser
XM_017003818.1:c.1705C>T	XP_016859307.1:p.Pro569Ser
XM_024452794.1:c.1504C>T	XP_024308562.1:p.Pro502Ser
XM_024452795.1:c.1504C>T	XP_024308563.1:p.Pro502Ser
NM_001371271.1:c.1504C>T	NP_001358200.1:p.Pro502Ser
NM_001374353.1:c.1453C>T MANE Select	NP_001361282.1:p.Pro485Ser
NM_001374354.1:c.1078C>T	NP_001361283.1:p.Pro360Ser
NM_005270.5:c.1504C>T	NP_005261.2:p.Pro502Ser