Canonical Allele Identifier: CA799419766
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs1170566182

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753113_85753115del , CM000666.2:g.85753113_85753115del GRCh38
NC_000004.11:g.86674266_86674268del , CM000666.1:g.86674266_86674268del GRCh37
NC_000004.10:g.86893290_86893292del NCBI36
NG_051627.1:g.282983_282985del

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+31141_268+31143del MANE Select ENSP00000378611.1:n.268+31141_268+31143de...
ENST00000395184.5:c.268+31141_268+31143del ENSP00000378611.1:n.268+31141_268+31143de...
ENST00000503995.5:c.268+31141_268+31143del ENSP00000423206.1:n.268+31141_268+31143de...
ENST00000512201.5:c.-18+31141_-18+31143del ENSP00000426105.1:n.-18+31141_-18+31143de...
NM_001025616.2:c.268+31141_268+31143del NP_001020787.2:n.268+31141_268+31143del
XM_005263263.3:c.268+31141_268+31143del XP_005263320.1:n.268+31141_268+31143del
XM_024454238.1:c.-18+31141_-18+31143del XP_024310006.1:n.-18+31141_-18+31143del
XM_024454239.1:c.-18+31141_-18+31143del XP_024310007.1:n.-18+31141_-18+31143del
NM_001025616.3:c.268+31141_268+31143del MANE Select NP_001020787.2:n.268+31141_268+31143del