Canonical Allele Identifier: CA1473827636
Gene: ARHGAP24 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753102T= , CM000666.2:g.85753102T= GRCh38
NC_000004.11:g.86674255T= , CM000666.1:g.86674255T= GRCh37
NC_000004.10:g.86893279T= NCBI36
NG_051627.1:g.282972T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395184.6:c.268+31130T= MANE Select ENSP00000378611.1:n.268+31130T=
ENST00000395184.5:c.268+31130T= ENSP00000378611.1:n.268+31130T=
ENST00000503995.5:c.268+31130T= ENSP00000423206.1:n.268+31130T=
ENST00000512201.5:c.-18+31130T= ENSP00000426105.1:n.-18+31130T=
NM_001025616.2:c.268+31130T= NP_001020787.2:n.268+31130T=
XM_005263263.3:c.268+31130T= XP_005263320.1:n.268+31130T=
XM_024454238.1:c.-18+31130T= XP_024310006.1:n.-18+31130T=
XM_024454239.1:c.-18+31130T= XP_024310007.1:n.-18+31130T=
NM_001025616.3:c.268+31130T= MANE Select NP_001020787.2:n.268+31130T=
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