Canonical Allele Identifier: CA2511135612

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85753069_85753070insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT , CM000666.2:g.85753069_85753070insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	GRCh38
NC_000004.11:g.86674222_86674223insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT , CM000666.1:g.86674222_86674223insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	GRCh37
NC_000004.10:g.86893246_86893247insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	NCBI36
NG_051627.1:g.282939_282940insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+31097_268+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT MANE Select	ENSP00000378611.1:n.268+31097_268+31098insTAAATCCTCTACAATAATG...
ENST00000395184.5:c.268+31097_268+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	ENSP00000378611.1:n.268+31097_268+31098insTAAATCCTCTACAATAATG...
ENST00000503995.5:c.268+31097_268+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	ENSP00000423206.1:n.268+31097_268+31098insTAAATCCTCTACAATAATG...
ENST00000512201.5:c.-18+31097_-18+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	ENSP00000426105.1:n.-18+31097_-18+31098insTAAATCCTCTACAATAATG...
NM_001025616.2:c.268+31097_268+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	NP_001020787.2:n.268+31097_268+31098insTAAATCCTCTACAATAATGAAA...
XM_005263263.3:c.268+31097_268+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	XP_005263320.1:n.268+31097_268+31098insTAAATCCTCTACAATAATGAAA...
XM_024454238.1:c.-18+31097_-18+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	XP_024310006.1:n.-18+31097_-18+31098insTAAATCCTCTACAATAATGAAA...
XM_024454239.1:c.-18+31097_-18+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT	XP_024310007.1:n.-18+31097_-18+31098insTAAATCCTCTACAATAATGAAA...
NM_001025616.3:c.268+31097_268+31098insTAAATCCTCTACAATAATGAAATTCTGGTAATGTTCAGAAGTAAGTATCTCTAGTGCCAGATTAATAT MANE Select	NP_001020787.2:n.268+31097_268+31098insTAAATCCTCTACAATAATGAAA...