Canonical Allele Identifier: CA1908306777

Gene: ARHGAP22

Linked Data

• dbSNP Id: rs10776614

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48555121T>A , CM000672.2:g.48555121T>A	GRCh38
NC_000010.10:g.49763166T>A , CM000672.1:g.49763166T>A	GRCh37
NC_000010.9:g.49433172T>A	NCBI36
NG_053158.1:g.106145A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000249601.9:c.322+342A>T MANE Select	ENSP00000249601.4:n.322+342A>T
ENST00000249601.8:c.322+342A>T	ENSP00000249601.4:n.322+342A>T
ENST00000374172.5:c.-54+342A>T	ENSP00000363287.1:n.-54+342A>T
ENST00000417912.6:c.322+342A>T	ENSP00000412461.2:n.322+342A>T
ENST00000435790.6:c.340+342A>T	ENSP00000416701.2:n.340+342A>T
ENST00000460425.1:c.340+342A>T	ENSP00000422663.1:n.340+342A>T
ENST00000471013.5:n.414+342A>T
ENST00000493012.2:n.261+342A>T
NM_001256024.1:c.322+342A>T	NP_001242953.1:n.322+342A>T
NM_001256025.2:c.340+342A>T	NP_001242954.1:n.340+342A>T
NM_021226.3:c.322+342A>T	NP_067049.2:n.322+342A>T
NR_045675.1:n.1208+342A>T
XM_011540002.1:c.340+342A>T	XP_011538304.1:n.340+342A>T
XM_011540003.1:c.340+342A>T	XP_011538305.1:n.340+342A>T
XM_011540004.1:c.340+342A>T	XP_011538306.1:n.340+342A>T
XM_011540006.1:c.340+342A>T	XP_011538308.1:n.340+342A>T
XM_011540013.1:c.340+342A>T	XP_011538315.1:n.340+342A>T
XM_011540014.1:c.340+342A>T	XP_011538316.1:n.340+342A>T
XM_011540015.1:c.340+342A>T	XP_011538317.1:n.340+342A>T
NM_001347735.1:c.322+342A>T	NP_001334664.1:n.322+342A>T
NM_001347738.1:c.340+342A>T	NP_001334667.1:n.340+342A>T
NR_144642.1:n.657+342A>T
NR_144643.1:n.657+342A>T
NR_144644.1:n.657+342A>T
NR_144645.1:n.657+342A>T
NR_144646.1:n.657+342A>T
XM_011540002.2:c.340+342A>T	XP_011538304.1:n.340+342A>T
XM_011540006.2:c.340+342A>T	XP_011538308.1:n.340+342A>T
XM_011540013.3:c.340+342A>T	XP_011538315.1:n.340+342A>T
XM_011540015.3:c.340+342A>T	XP_011538317.1:n.340+342A>T
XM_017016476.1:c.322+342A>T	XP_016871965.1:n.322+342A>T
XM_024448099.1:c.340+342A>T	XP_024303867.1:n.340+342A>T
XM_024448100.1:c.340+342A>T	XP_024303868.1:n.340+342A>T
XM_024448101.1:c.-248+342A>T	XP_024303869.1:n.-248+342A>T
XM_024448102.1:c.340+342A>T	XP_024303870.1:n.340+342A>T
XM_024448103.1:c.340+342A>T	XP_024303871.1:n.340+342A>T
XM_024448104.1:c.340+342A>T	XP_024303872.1:n.340+342A>T
XM_024448105.1:c.340+342A>T	XP_024303873.1:n.340+342A>T
XR_001747166.2:n.537+342A>T
XR_002956998.1:n.359+342A>T
XR_002956999.1:n.537+342A>T
XR_002957000.1:n.537+342A>T
XR_002957001.1:n.537+342A>T
XR_002957002.1:n.537+342A>T
XR_002957003.1:n.537+342A>T
XR_002957004.1:n.537+342A>T
NM_001256024.2:c.322+342A>T	NP_001242953.1:n.322+342A>T
NM_001256025.3:c.340+342A>T	NP_001242954.1:n.340+342A>T
NM_001347735.2:c.322+342A>T	NP_001334664.1:n.322+342A>T
NM_001347738.2:c.340+342A>T	NP_001334667.1:n.340+342A>T
NM_021226.4:c.322+342A>T MANE Select	NP_067049.2:n.322+342A>T
NR_045675.2:n.1208+342A>T
NR_144642.2:n.599+342A>T
NR_144643.2:n.599+342A>T
NR_144644.2:n.599+342A>T
NR_144645.2:n.599+342A>T
NR_144646.2:n.599+342A>T