Canonical Allele Identifier: CA1473827183

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85752858_85752859delinsAT , CM000666.2:g.85752858_85752859delinsAT	GRCh38
NC_000004.11:g.86674011_86674012delinsAT , CM000666.1:g.86674011_86674012delinsAT	GRCh37
NC_000004.10:g.86893035_86893036delinsAT	NCBI36
NG_051627.1:g.282728_282729delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+30886_268+30887delinsAT MANE Select	ENSP00000378611.1:n.268+30886_268+30887delinsAT
ENST00000395184.5:c.268+30886_268+30887delinsAT	ENSP00000378611.1:n.268+30886_268+30887delinsAT
ENST00000503995.5:c.268+30886_268+30887delinsAT	ENSP00000423206.1:n.268+30886_268+30887delinsAT
ENST00000512201.5:c.-18+30886_-18+30887delinsAT	ENSP00000426105.1:n.-18+30886_-18+30887delinsAT
NM_001025616.2:c.268+30886_268+30887delinsAT	NP_001020787.2:n.268+30886_268+30887delinsAT
XM_005263263.3:c.268+30886_268+30887delinsAT	XP_005263320.1:n.268+30886_268+30887delinsAT
XM_024454238.1:c.-18+30886_-18+30887delinsAT	XP_024310006.1:n.-18+30886_-18+30887delinsAT
XM_024454239.1:c.-18+30886_-18+30887delinsAT	XP_024310007.1:n.-18+30886_-18+30887delinsAT
NM_001025616.3:c.268+30886_268+30887delinsAT MANE Select	NP_001020787.2:n.268+30886_268+30887delinsAT