Canonical Allele Identifier: CA1473785607

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85730275_85730276delinsTC , CM000666.2:g.85730275_85730276delinsTC	GRCh38
NC_000004.11:g.86651428_86651429delinsTC , CM000666.1:g.86651428_86651429delinsTC	GRCh37
NC_000004.10:g.86870452_86870453delinsTC	NCBI36
NG_051627.1:g.260145_260146delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000395184.6:c.268+8303_268+8304delinsTC MANE Select	ENSP00000378611.1:n.268+8303_268+8304deli...
ENST00000395184.5:c.268+8303_268+8304delinsTC	ENSP00000378611.1:n.268+8303_268+8304deli...
ENST00000503995.5:c.268+8303_268+8304delinsTC	ENSP00000423206.1:n.268+8303_268+8304deli...
ENST00000512201.5:c.-18+8303_-18+8304delinsTC	ENSP00000426105.1:n.-18+8303_-18+8304deli...
NM_001025616.2:c.268+8303_268+8304delinsTC	NP_001020787.2:n.268+8303_268+8304delinsT...
XM_005263263.3:c.268+8303_268+8304delinsTC	XP_005263320.1:n.268+8303_268+8304delinsT...
XM_024454238.1:c.-18+8303_-18+8304delinsTC	XP_024310006.1:n.-18+8303_-18+8304delinsT...
XM_024454239.1:c.-18+8303_-18+8304delinsTC	XP_024310007.1:n.-18+8303_-18+8304delinsT...
NM_001025616.3:c.268+8303_268+8304delinsTC MANE Select	NP_001020787.2:n.268+8303_268+8304delinsT...