Canonical Allele Identifier: CA1473785771

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85730406_85730410delinsGTTTT , CM000666.2:g.85730406_85730410delinsGTTTT	GRCh38
NC_000004.11:g.86651559_86651563delinsGTTTT , CM000666.1:g.86651559_86651563delinsGTTTT	GRCh37
NC_000004.10:g.86870583_86870587delinsGTTTT	NCBI36
NG_051627.1:g.260276_260280delinsGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+8434_268+8438delinsGTTTT MANE Select	ENSP00000378611.1:n.268+8434_268+8438delinsGTTTT
ENST00000395184.5:c.268+8434_268+8438delinsGTTTT	ENSP00000378611.1:n.268+8434_268+8438delinsGTTTT
ENST00000503995.5:c.268+8434_268+8438delinsGTTTT	ENSP00000423206.1:n.268+8434_268+8438delinsGTTTT
ENST00000512201.5:c.-18+8434_-18+8438delinsGTTTT	ENSP00000426105.1:n.-18+8434_-18+8438delinsGTTTT
NM_001025616.2:c.268+8434_268+8438delinsGTTTT	NP_001020787.2:n.268+8434_268+8438delinsGTTTT
XM_005263263.3:c.268+8434_268+8438delinsGTTTT	XP_005263320.1:n.268+8434_268+8438delinsGTTTT
XM_024454238.1:c.-18+8434_-18+8438delinsGTTTT	XP_024310006.1:n.-18+8434_-18+8438delinsGTTTT
XM_024454239.1:c.-18+8434_-18+8438delinsGTTTT	XP_024310007.1:n.-18+8434_-18+8438delinsGTTTT
NM_001025616.3:c.268+8434_268+8438delinsGTTTT MANE Select	NP_001020787.2:n.268+8434_268+8438delinsGTTTT