Canonical Allele Identifier: CA1908284632

Gene: ARHGAP22

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48491914C>G , CM000672.2:g.48491914C>G	GRCh38
NC_000010.10:g.49699957C>G , CM000672.1:g.49699957C>G	GRCh37
NC_000010.9:g.49369963C>G	NCBI36
NG_053158.1:g.169352G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249601.9:c.323-12150G>C MANE Select	ENSP00000249601.4:n.323-12150G>C
ENST00000249601.8:c.323-12150G>C	ENSP00000249601.4:n.323-12150G>C
ENST00000374170.5:c.53-12150G>C	ENSP00000363285.1:n.53-12150G>C
ENST00000374172.5:c.-53-12150G>C	ENSP00000363287.1:n.-53-12150G>C
ENST00000417247.6:c.52+1525G>C	ENSP00000410054.2:n.52+1525G>C
ENST00000417912.6:c.323-12150G>C	ENSP00000412461.2:n.323-12150G>C
ENST00000435790.6:c.341-12150G>C	ENSP00000416701.2:n.341-12150G>C
ENST00000460425.1:c.341-12150G>C	ENSP00000422663.1:n.341-12150G>C
ENST00000471013.5:n.415-36780G>C
NM_001256024.1:c.323-12150G>C	NP_001242953.1:n.323-12150G>C
NM_001256025.2:c.341-12150G>C	NP_001242954.1:n.341-12150G>C
NM_001256026.1:c.52+1525G>C	NP_001242955.1:n.52+1525G>C
NM_021226.3:c.323-12150G>C	NP_067049.2:n.323-12150G>C
NR_045675.1:n.1209-12150G>C
XM_005270014.2:c.53-12150G>C	XP_005270071.1:n.53-12150G>C
XM_011540002.1:c.341-12150G>C	XP_011538304.1:n.341-12150G>C
XM_011540003.1:c.341-12150G>C	XP_011538305.1:n.341-12150G>C
XM_011540004.1:c.341-12150G>C	XP_011538306.1:n.341-12150G>C
XM_011540005.1:c.52+1525G>C	XP_011538307.1:n.52+1525G>C
XM_011540006.1:c.341-32023G>C	XP_011538308.1:n.341-32023G>C
XM_011540007.1:c.92-12150G>C	XP_011538309.1:n.92-12150G>C
XM_011540011.1:c.53-32023G>C	XP_011538313.1:n.53-32023G>C
XM_011540013.1:c.341-12150G>C	XP_011538315.1:n.341-12150G>C
XM_011540014.1:c.341-12150G>C	XP_011538316.1:n.341-12150G>C
XM_011540015.1:c.341-12150G>C	XP_011538317.1:n.341-12150G>C
NM_001347735.1:c.323-32023G>C	NP_001334664.1:n.323-32023G>C
NM_001347738.1:c.341-12150G>C	NP_001334667.1:n.341-12150G>C
NR_144642.1:n.658-12150G>C
NR_144643.1:n.658-12150G>C
NR_144644.1:n.658-32023G>C
NR_144645.1:n.658-12150G>C
NR_144646.1:n.658-12150G>C
XM_005270014.3:c.53-12150G>C	XP_005270071.1:n.53-12150G>C
XM_011540002.2:c.341-12150G>C	XP_011538304.1:n.341-12150G>C
XM_011540006.2:c.341-32023G>C	XP_011538308.1:n.341-32023G>C
XM_011540011.2:c.53-32023G>C	XP_011538313.1:n.53-32023G>C
XM_011540013.3:c.341-12150G>C	XP_011538315.1:n.341-12150G>C
XM_011540015.3:c.341-12150G>C	XP_011538317.1:n.341-12150G>C
XM_017016476.1:c.323-12150G>C	XP_016871965.1:n.323-12150G>C
XM_024448099.1:c.341-12150G>C	XP_024303867.1:n.341-12150G>C
XM_024448100.1:c.341-12150G>C	XP_024303868.1:n.341-12150G>C
XM_024448101.1:c.-247-36780G>C	XP_024303869.1:n.-247-36780G>C
XM_024448103.1:c.341-36780G>C	XP_024303871.1:n.341-36780G>C
XR_001747166.2:n.538-12150G>C
XR_002956998.1:n.360-12150G>C
XR_002956999.1:n.538-12150G>C
XR_002957000.1:n.538-12150G>C
XR_002957001.1:n.538-12150G>C
XR_002957002.1:n.538-12150G>C
XR_002957003.1:n.538-12150G>C
XR_002957004.1:n.538-36780G>C
NM_001256024.2:c.323-12150G>C	NP_001242953.1:n.323-12150G>C
NM_001256025.3:c.341-12150G>C	NP_001242954.1:n.341-12150G>C
NM_001256026.2:c.52+1525G>C	NP_001242955.1:n.52+1525G>C
NM_001347735.2:c.323-32023G>C	NP_001334664.1:n.323-32023G>C
NM_001347738.2:c.341-12150G>C	NP_001334667.1:n.341-12150G>C
NM_021226.4:c.323-12150G>C MANE Select	NP_067049.2:n.323-12150G>C
NR_045675.2:n.1209-12150G>C
NR_144642.2:n.600-12150G>C
NR_144643.2:n.600-12150G>C
NR_144644.2:n.600-32023G>C
NR_144645.2:n.600-12150G>C
NR_144646.2:n.600-12150G>C