Canonical Allele Identifier: CA1473827552
Gene: ARHGAP24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753054_85753055delinsGT , CM000666.2:g.85753054_85753055delinsGT GRCh38
NC_000004.11:g.86674207_86674208delinsGT , CM000666.1:g.86674207_86674208delinsGT GRCh37
NC_000004.10:g.86893231_86893232delinsGT NCBI36
NG_051627.1:g.282924_282925delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+31082_268+31083delinsGT MANE Select ENSP00000378611.1:n.268+31082_268+31083de...
ENST00000395184.5:c.268+31082_268+31083delinsGT ENSP00000378611.1:n.268+31082_268+31083de...
ENST00000503995.5:c.268+31082_268+31083delinsGT ENSP00000423206.1:n.268+31082_268+31083de...
ENST00000512201.5:c.-18+31082_-18+31083delinsGT ENSP00000426105.1:n.-18+31082_-18+31083de...
NM_001025616.2:c.268+31082_268+31083delinsGT NP_001020787.2:n.268+31082_268+31083delin...
XM_005263263.3:c.268+31082_268+31083delinsGT XP_005263320.1:n.268+31082_268+31083delin...
XM_024454238.1:c.-18+31082_-18+31083delinsGT XP_024310006.1:n.-18+31082_-18+31083delin...
XM_024454239.1:c.-18+31082_-18+31083delinsGT XP_024310007.1:n.-18+31082_-18+31083delin...
NM_001025616.3:c.268+31082_268+31083delinsGT MANE Select NP_001020787.2:n.268+31082_268+31083delin...