Canonical Allele Identifier: CA1473785561

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85730253T= , CM000666.2:g.85730253T=	GRCh38
NC_000004.11:g.86651406T= , CM000666.1:g.86651406T=	GRCh37
NC_000004.10:g.86870430T=	NCBI36
NG_051627.1:g.260123T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395184.6:c.268+8281T= MANE Select	ENSP00000378611.1:n.268+8281T=
ENST00000395184.5:c.268+8281T=	ENSP00000378611.1:n.268+8281T=
ENST00000503995.5:c.268+8281T=	ENSP00000423206.1:n.268+8281T=
ENST00000512201.5:c.-18+8281T=	ENSP00000426105.1:n.-18+8281T=
NM_001025616.2:c.268+8281T=	NP_001020787.2:n.268+8281T=
XM_005263263.3:c.268+8281T=	XP_005263320.1:n.268+8281T=
XM_024454238.1:c.-18+8281T=	XP_024310006.1:n.-18+8281T=
XM_024454239.1:c.-18+8281T=	XP_024310007.1:n.-18+8281T=
NM_001025616.3:c.268+8281T= MANE Select	NP_001020787.2:n.268+8281T=