Canonical Allele Identifier: CA1473827050

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85752754_85752755delinsTA , CM000666.2:g.85752754_85752755delinsTA	GRCh38
NC_000004.11:g.86673907_86673908delinsTA , CM000666.1:g.86673907_86673908delinsTA	GRCh37
NC_000004.10:g.86892931_86892932delinsTA	NCBI36
NG_051627.1:g.282624_282625delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+30782_268+30783delinsTA MANE Select	ENSP00000378611.1:n.268+30782_268+30783delinsTA
ENST00000395184.5:c.268+30782_268+30783delinsTA	ENSP00000378611.1:n.268+30782_268+30783delinsTA
ENST00000503995.5:c.268+30782_268+30783delinsTA	ENSP00000423206.1:n.268+30782_268+30783delinsTA
ENST00000512201.5:c.-18+30782_-18+30783delinsTA	ENSP00000426105.1:n.-18+30782_-18+30783delinsTA
NM_001025616.2:c.268+30782_268+30783delinsTA	NP_001020787.2:n.268+30782_268+30783delinsTA
XM_005263263.3:c.268+30782_268+30783delinsTA	XP_005263320.1:n.268+30782_268+30783delinsTA
XM_024454238.1:c.-18+30782_-18+30783delinsTA	XP_024310006.1:n.-18+30782_-18+30783delinsTA
XM_024454239.1:c.-18+30782_-18+30783delinsTA	XP_024310007.1:n.-18+30782_-18+30783delinsTA
NM_001025616.3:c.268+30782_268+30783delinsTA MANE Select	NP_001020787.2:n.268+30782_268+30783delinsTA