Canonical Allele Identifier: CA799419674

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs1473258208
• gnomAD v3: 4-85752818-TTGCTTGG-T
• gnomAD v4: 4-85752818-TTGCTTGG-T
• MyVariant Identifiers: chr4:g.86673972_86673978del (hg19) ; chr4:g.85752819_85752825del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85752819_85752825del , CM000666.2:g.85752819_85752825del	GRCh38
NC_000004.11:g.86673972_86673978del , CM000666.1:g.86673972_86673978del	GRCh37
NC_000004.10:g.86892996_86893002del	NCBI36
NG_051627.1:g.282689_282695del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+30847_268+30853del MANE Select	ENSP00000378611.1:n.268+30847_268+30853del
ENST00000395184.5:c.268+30847_268+30853del	ENSP00000378611.1:n.268+30847_268+30853del
ENST00000503995.5:c.268+30847_268+30853del	ENSP00000423206.1:n.268+30847_268+30853del
ENST00000512201.5:c.-18+30847_-18+30853del	ENSP00000426105.1:n.-18+30847_-18+30853del
NM_001025616.2:c.268+30847_268+30853del	NP_001020787.2:n.268+30847_268+30853del
XM_005263263.3:c.268+30847_268+30853del	XP_005263320.1:n.268+30847_268+30853del
XM_024454238.1:c.-18+30847_-18+30853del	XP_024310006.1:n.-18+30847_-18+30853del
XM_024454239.1:c.-18+30847_-18+30853del	XP_024310007.1:n.-18+30847_-18+30853del
NM_001025616.3:c.268+30847_268+30853del MANE Select	NP_001020787.2:n.268+30847_268+30853del