Canonical Allele Identifier: CA1473827668

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85753121_85753122delinsTG , CM000666.2:g.85753121_85753122delinsTG	GRCh38
NC_000004.11:g.86674274_86674275delinsTG , CM000666.1:g.86674274_86674275delinsTG	GRCh37
NC_000004.10:g.86893298_86893299delinsTG	NCBI36
NG_051627.1:g.282991_282992delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+31149_268+31150delinsTG MANE Select	ENSP00000378611.1:n.268+31149_268+31150delinsTG
ENST00000395184.5:c.268+31149_268+31150delinsTG	ENSP00000378611.1:n.268+31149_268+31150delinsTG
ENST00000503995.5:c.268+31149_268+31150delinsTG	ENSP00000423206.1:n.268+31149_268+31150delinsTG
ENST00000512201.5:c.-18+31149_-18+31150delinsTG	ENSP00000426105.1:n.-18+31149_-18+31150delinsTG
NM_001025616.2:c.268+31149_268+31150delinsTG	NP_001020787.2:n.268+31149_268+31150delinsTG
XM_005263263.3:c.268+31149_268+31150delinsTG	XP_005263320.1:n.268+31149_268+31150delinsTG
XM_024454238.1:c.-18+31149_-18+31150delinsTG	XP_024310006.1:n.-18+31149_-18+31150delinsTG
XM_024454239.1:c.-18+31149_-18+31150delinsTG	XP_024310007.1:n.-18+31149_-18+31150delinsTG
NM_001025616.3:c.268+31149_268+31150delinsTG MANE Select	NP_001020787.2:n.268+31149_268+31150delinsTG