Canonical Allele Identifier: CA917243279
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs1560616147

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753135dup , CM000666.2:g.85753135dup GRCh38
NC_000004.11:g.86674288dup , CM000666.1:g.86674288dup GRCh37
NC_000004.10:g.86893312dup NCBI36
NG_051627.1:g.283005dup

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+31163dup MANE Select ENSP00000378611.1:n.268+31163dup
ENST00000395184.5:c.268+31163dup ENSP00000378611.1:n.268+31163dup
ENST00000503995.5:c.268+31163dup ENSP00000423206.1:n.268+31163dup
ENST00000512201.5:c.-18+31163dup ENSP00000426105.1:n.-18+31163dup
NM_001025616.2:c.268+31163dup NP_001020787.2:n.268+31163dup
XM_005263263.3:c.268+31163dup XP_005263320.1:n.268+31163dup
XM_024454238.1:c.-18+31163dup XP_024310006.1:n.-18+31163dup
XM_024454239.1:c.-18+31163dup XP_024310007.1:n.-18+31163dup
NM_001025616.3:c.268+31163dup MANE Select NP_001020787.2:n.268+31163dup