Canonical Allele Identifier: CA1473827702

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85753148C= , CM000666.2:g.85753148C=	GRCh38
NC_000004.11:g.86674301C= , CM000666.1:g.86674301C=	GRCh37
NC_000004.10:g.86893325C=	NCBI36
NG_051627.1:g.283018C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+31176C= MANE Select	ENSP00000378611.1:n.268+31176C=
ENST00000395184.5:c.268+31176C=	ENSP00000378611.1:n.268+31176C=
ENST00000503995.5:c.268+31176C=	ENSP00000423206.1:n.268+31176C=
ENST00000512201.5:c.-18+31176C=	ENSP00000426105.1:n.-18+31176C=
NM_001025616.2:c.268+31176C=	NP_001020787.2:n.268+31176C=
XM_005263263.3:c.268+31176C=	XP_005263320.1:n.268+31176C=
XM_024454238.1:c.-18+31176C=	XP_024310006.1:n.-18+31176C=
XM_024454239.1:c.-18+31176C=	XP_024310007.1:n.-18+31176C=
NM_001025616.3:c.268+31176C= MANE Select	NP_001020787.2:n.268+31176C=