Canonical Allele Identifier: CA1473827589

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85753071G= , CM000666.2:g.85753071G=	GRCh38
NC_000004.11:g.86674224G= , CM000666.1:g.86674224G=	GRCh37
NC_000004.10:g.86893248G=	NCBI36
NG_051627.1:g.282941G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+31099G= MANE Select	ENSP00000378611.1:n.268+31099G=
ENST00000395184.5:c.268+31099G=	ENSP00000378611.1:n.268+31099G=
ENST00000503995.5:c.268+31099G=	ENSP00000423206.1:n.268+31099G=
ENST00000512201.5:c.-18+31099G=	ENSP00000426105.1:n.-18+31099G=
NM_001025616.2:c.268+31099G=	NP_001020787.2:n.268+31099G=
XM_005263263.3:c.268+31099G=	XP_005263320.1:n.268+31099G=
XM_024454238.1:c.-18+31099G=	XP_024310006.1:n.-18+31099G=
XM_024454239.1:c.-18+31099G=	XP_024310007.1:n.-18+31099G=
NM_001025616.3:c.268+31099G= MANE Select	NP_001020787.2:n.268+31099G=