Canonical Allele Identifier: CA2840490423

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85753090_85753096del , CM000666.2:g.85753090_85753096del	GRCh38
NC_000004.11:g.86674243_86674249del , CM000666.1:g.86674243_86674249del	GRCh37
NC_000004.10:g.86893267_86893273del	NCBI36
NG_051627.1:g.282960_282966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+31118_268+31124del MANE Select	ENSP00000378611.1:n.268+31118_268+31124del
ENST00000395184.5:c.268+31118_268+31124del	ENSP00000378611.1:n.268+31118_268+31124del
ENST00000503995.5:c.268+31118_268+31124del	ENSP00000423206.1:n.268+31118_268+31124del
ENST00000512201.5:c.-18+31118_-18+31124del	ENSP00000426105.1:n.-18+31118_-18+31124del
NM_001025616.2:c.268+31118_268+31124del	NP_001020787.2:n.268+31118_268+31124del
XM_005263263.3:c.268+31118_268+31124del	XP_005263320.1:n.268+31118_268+31124del
XM_024454238.1:c.-18+31118_-18+31124del	XP_024310006.1:n.-18+31118_-18+31124del
XM_024454239.1:c.-18+31118_-18+31124del	XP_024310007.1:n.-18+31118_-18+31124del
NM_001025616.3:c.268+31118_268+31124del MANE Select	NP_001020787.2:n.268+31118_268+31124del