Canonical Allele Identifier: CA101274866
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs796211558

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85730145_85730146delinsGG , CM000666.2:g.85730145_85730146delinsGG GRCh38
NC_000004.11:g.86651298_86651299delinsGG , CM000666.1:g.86651298_86651299delinsGG GRCh37
NC_000004.10:g.86870322_86870323delinsGG NCBI36
NG_051627.1:g.260015_260016delinsGG

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+8173_268+8174delinsGG MANE Select ENSP00000378611.1:n.268+8173_268+8174deli...
ENST00000395184.5:c.268+8173_268+8174delinsGG ENSP00000378611.1:n.268+8173_268+8174deli...
ENST00000503995.5:c.268+8173_268+8174delinsGG ENSP00000423206.1:n.268+8173_268+8174deli...
ENST00000512201.5:c.-18+8173_-18+8174delinsGG ENSP00000426105.1:n.-18+8173_-18+8174deli...
NM_001025616.2:c.268+8173_268+8174delinsGG NP_001020787.2:n.268+8173_268+8174delinsG...
XM_005263263.3:c.268+8173_268+8174delinsGG XP_005263320.1:n.268+8173_268+8174delinsG...
XM_024454238.1:c.-18+8173_-18+8174delinsGG XP_024310006.1:n.-18+8173_-18+8174delinsG...
XM_024454239.1:c.-18+8173_-18+8174delinsGG XP_024310007.1:n.-18+8173_-18+8174delinsG...
NM_001025616.3:c.268+8173_268+8174delinsGG MANE Select NP_001020787.2:n.268+8173_268+8174delinsG...