Canonical Allele Identifier: CA101277309
Gene: ARHGAP24 HGNC NCBI

Linked Data

dbSNP Id: rs548964406
gnomAD v2: 4-86674299-G-A
gnomAD v3: 4-85753146-G-A
gnomAD v4: 4-85753146-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753146G>A , CM000666.2:g.85753146G>A GRCh38
NC_000004.11:g.86674299G>A , CM000666.1:g.86674299G>A GRCh37
NC_000004.10:g.86893323G>A NCBI36
NG_051627.1:g.283016G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395184.6:c.268+31174G>A MANE Select ENSP00000378611.1:n.268+31174G>A
ENST00000395184.5:c.268+31174G>A ENSP00000378611.1:n.268+31174G>A
ENST00000503995.5:c.268+31174G>A ENSP00000423206.1:n.268+31174G>A
ENST00000512201.5:c.-18+31174G>A ENSP00000426105.1:n.-18+31174G>A
NM_001025616.2:c.268+31174G>A NP_001020787.2:n.268+31174G>A
XM_005263263.3:c.268+31174G>A XP_005263320.1:n.268+31174G>A
XM_024454238.1:c.-18+31174G>A XP_024310006.1:n.-18+31174G>A
XM_024454239.1:c.-18+31174G>A XP_024310007.1:n.-18+31174G>A
NM_001025616.3:c.268+31174G>A MANE Select NP_001020787.2:n.268+31174G>A