Canonical Allele Identifier: CA12117832

Gene: IQGAP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76625147A>G , CM000667.2:g.76625147A>G	GRCh38
NC_000005.9:g.75920972A>G , CM000667.1:g.75920972A>G	GRCh37
NC_000005.8:g.75956728A>G	NCBI36
NG_053128.1:g.226893A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685113.1:n.269-2263A>G
ENST00000685564.1:c.-34-2263A>G	ENSP00000510681.1:n.-34-2263A>G
ENST00000274364.11:c.1522-2263A>G MANE Select	ENSP00000274364.6:n.1522-2263A>G
ENST00000274364.10:c.1522-2263A>G	ENSP00000274364.6:n.1522-2263A>G
ENST00000379730.7:c.1372-2263A>G	ENSP00000442313.2:n.1372-2263A>G
ENST00000396234.7:c.181-2263A>G	ENSP00000379535.3:n.181-2263A>G
ENST00000502745.5:c.181-2263A>G	ENSP00000426027.1:n.181-2263A>G
ENST00000504254.5:c.*266+662A>G	ENSP00000423258.1:n.*266+662A>G
ENST00000505766.5:c.1372-2263A>G	ENSP00000421097.1:n.1372-2263A>G
ENST00000509074.5:c.181-2263A>G	ENSP00000425351.1:n.181-2263A>G
ENST00000513534.1:c.181-2263A>G	ENSP00000421319.1:n.181-2263A>G
ENST00000514001.5:c.181-2263A>G	ENSP00000422661.1:n.181-2263A>G
ENST00000514350.5:c.1441-2263A>G	ENSP00000423672.1:n.1441-2263A>G
ENST00000515505.1:n.94-2263A>G
NM_001285460.1:c.1372-2263A>G	NP_001272389.1:n.1372-2263A>G
NM_001285461.1:c.181-2263A>G	NP_001272390.1:n.181-2263A>G
NM_001285462.1:c.181-2263A>G	NP_001272391.1:n.181-2263A>G
NM_006633.3:c.1522-2263A>G	NP_006624.2:n.1522-2263A>G
XM_005248410.1:c.1441-2263A>G	XP_005248467.1:n.1441-2263A>G
XM_005248414.1:c.181-2263A>G	XP_005248471.1:n.181-2263A>G
XM_011543107.1:c.1441-2263A>G	XP_011541409.1:n.1441-2263A>G
XM_011543108.1:c.181-2263A>G	XP_011541410.1:n.181-2263A>G
XM_005248410.3:c.1441-2263A>G	XP_005248467.1:n.1441-2263A>G
XM_005248414.2:c.181-2263A>G	XP_005248471.1:n.181-2263A>G
XM_011543108.2:c.181-2263A>G	XP_011541410.1:n.181-2263A>G
XM_017008960.1:c.1522-2263A>G	XP_016864449.1:n.1522-2263A>G
XM_024454336.1:c.1516-2263A>G	XP_024310104.1:n.1516-2263A>G
XM_024454337.1:c.1441-2263A>G	XP_024310105.1:n.1441-2263A>G
NM_006633.4:c.1522-2263A>G	NP_006624.2:n.1522-2263A>G
NM_001285460.2:c.1372-2263A>G	NP_001272389.2:n.1372-2263A>G
NM_001285461.2:c.181-2263A>G	NP_001272390.2:n.181-2263A>G
NM_001285462.2:c.181-2263A>G	NP_001272391.2:n.181-2263A>G
NM_006633.5:c.1522-2263A>G MANE Select	NP_006624.3:n.1522-2263A>G