Canonical Allele Identifier: CA2838197115

Gene: ARHGEF2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155957915G>T , CM000663.2:g.155957915G>T	GRCh38
NC_000001.10:g.155927706G>T , CM000663.1:g.155927706G>T	GRCh37
NC_000001.9:g.154194330G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696600.1:c.*1208-33C>A	ENSP00000512745.1:n.*1208-33C>A
ENST00000696601.1:c.1549-33C>A	ENSP00000512746.1:n.1549-33C>A
ENST00000361247.9:c.1546-33C>A MANE Select	ENSP00000354837.4:n.1546-33C>A
ENST00000673475.1:c.1975-33C>A	ENSP00000500802.1:n.1975-33C>A
ENST00000313667.8:c.1543-33C>A	ENSP00000314787.4:n.1543-33C>A
ENST00000313695.11:c.1462-33C>A	ENSP00000315325.7:n.1462-33C>A
ENST00000361247.8:c.1546-33C>A	ENSP00000354837.4:n.1546-33C>A
ENST00000462460.6:c.1681-33C>A	ENSP00000476916.1:n.1681-33C>A
ENST00000470975.2:n.375-33C>A
ENST00000474428.6:n.476-33C>A
ENST00000477754.2:n.658-10835C>A
NM_001162383.1:c.1546-33C>A	NP_001155855.1:n.1546-33C>A
NM_001162384.1:c.1543-33C>A	NP_001155856.1:n.1543-33C>A
NM_004723.3:c.1462-33C>A	NP_004714.2:n.1462-33C>A
XM_005245587.1:c.1546-33C>A	XP_005245644.1:n.1546-33C>A
XM_005245588.1:c.1543-33C>A	XP_005245645.1:n.1543-33C>A
XM_005245589.3:c.1522-33C>A	XP_005245646.1:n.1522-33C>A
XM_005245590.2:c.1501-33C>A	XP_005245647.1:n.1501-33C>A
XM_005245591.2:c.1501-33C>A	XP_005245648.1:n.1501-33C>A
XM_005245592.1:c.1465-33C>A	XP_005245649.1:n.1465-33C>A
XM_005245593.3:c.1465-33C>A	XP_005245650.1:n.1465-33C>A
XM_005245594.1:c.1465-33C>A	XP_005245651.1:n.1465-33C>A
XM_006711622.2:c.1495-33C>A	XP_006711685.1:n.1495-33C>A
XM_006711623.2:c.1318-33C>A	XP_006711686.1:n.1318-33C>A
XM_006711624.2:c.1318-33C>A	XP_006711687.1:n.1318-33C>A
XM_006711625.2:c.1318-33C>A	XP_006711688.1:n.1318-33C>A
XM_006711626.1:c.1318-33C>A	XP_006711689.1:n.1318-33C>A
XM_011510136.1:c.1498-33C>A	XP_011508438.1:n.1498-33C>A
XM_011510137.1:c.1501-33C>A	XP_011508439.1:n.1501-33C>A
XM_011510138.1:c.1681-33C>A	XP_011508440.1:n.1681-33C>A
XM_011510139.1:c.1975-33C>A	XP_011508441.1:n.1975-33C>A
XM_011510140.1:c.1681-33C>A	XP_011508442.1:n.1681-33C>A
XM_011510141.1:c.1534-33C>A	XP_011508443.1:n.1534-33C>A
XM_011510142.1:c.1678-33C>A	XP_011508444.1:n.1678-33C>A
XM_011510143.1:c.1009-33C>A	XP_011508445.1:n.1009-33C>A
NM_001350110.1:c.1465-33C>A	NP_001337039.1:n.1465-33C>A
NM_001350111.1:c.1465-33C>A	NP_001337040.1:n.1465-33C>A
NM_001350112.1:c.1492-33C>A	NP_001337041.1:n.1492-33C>A
XM_005245587.3:c.1546-33C>A	XP_005245644.1:n.1546-33C>A
XM_005245588.3:c.1543-33C>A	XP_005245645.1:n.1543-33C>A
XM_005245589.5:c.1522-33C>A	XP_005245646.1:n.1522-33C>A
XM_005245590.4:c.1501-33C>A	XP_005245647.1:n.1501-33C>A
XM_005245591.4:c.1501-33C>A	XP_005245648.1:n.1501-33C>A
XM_005245594.3:c.1465-33C>A	XP_005245651.1:n.1465-33C>A
XM_006711622.4:c.1495-33C>A	XP_006711685.1:n.1495-33C>A
XM_006711623.4:c.1318-33C>A	XP_006711686.1:n.1318-33C>A
XM_006711624.4:c.1318-33C>A	XP_006711687.1:n.1318-33C>A
XM_006711625.4:c.1318-33C>A	XP_006711688.1:n.1318-33C>A
XM_006711626.3:c.1318-33C>A	XP_006711689.1:n.1318-33C>A
XM_011510136.3:c.1972-33C>A	XP_011508438.2:n.1972-33C>A
XM_011510137.3:c.1975-33C>A	XP_011508439.2:n.1975-33C>A
XM_011510139.3:c.1975-33C>A	XP_011508441.1:n.1975-33C>A
XM_011510143.3:c.1009-33C>A	XP_011508445.1:n.1009-33C>A
XM_017002794.2:c.1972-33C>A	XP_016858283.1:n.1972-33C>A
XM_017002795.2:c.1519-33C>A	XP_016858284.1:n.1519-33C>A
XM_017002797.2:c.1462-33C>A	XP_016858286.1:n.1462-33C>A
XM_017002798.2:c.1318-33C>A	XP_016858287.1:n.1318-33C>A
XM_024450815.1:c.1318-33C>A	XP_024306583.1:n.1318-33C>A
XM_024450823.1:c.1315-33C>A	XP_024306591.1:n.1315-33C>A
NM_001162383.2:c.1546-33C>A MANE Select	NP_001155855.1:n.1546-33C>A
NM_001162384.2:c.1543-33C>A	NP_001155856.1:n.1543-33C>A
NM_001350110.2:c.1465-33C>A	NP_001337039.1:n.1465-33C>A
NM_001350111.2:c.1465-33C>A	NP_001337040.1:n.1465-33C>A
NM_001350112.2:c.1492-33C>A	NP_001337041.1:n.1492-33C>A
NM_004723.4:c.1462-33C>A	NP_004714.2:n.1462-33C>A