Canonical Allele Identifier: CA1473873703

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85794159G= , CM000666.2:g.85794159G=	GRCh38
NC_000004.11:g.86715312G= , CM000666.1:g.86715312G=	GRCh37
NC_000004.10:g.86934336G=	NCBI36
NG_051627.1:g.324029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+72187G= MANE Select	ENSP00000378611.1:n.268+72187G=
ENST00000395183.6:c.-18+15194G=	ENSP00000378610.2:n.-18+15194G=
ENST00000395184.5:c.268+72187G=	ENSP00000378611.1:n.268+72187G=
ENST00000503995.5:c.268+72187G=	ENSP00000423206.1:n.268+72187G=
ENST00000512201.5:c.-18+72187G=	ENSP00000426105.1:n.-18+72187G=
NM_001025616.2:c.268+72187G=	NP_001020787.2:n.268+72187G=
NM_001042669.1:c.-18+15194G=	NP_001036134.1:n.-18+15194G=
XM_005263263.3:c.268+72187G=	XP_005263320.1:n.268+72187G=
NM_001346093.1:c.-104+15194G=	NP_001333022.1:n.-104+15194G=
XM_024454238.1:c.-18+72187G=	XP_024310006.1:n.-18+72187G=
XM_024454239.1:c.-18+72187G=	XP_024310007.1:n.-18+72187G=
NM_001025616.3:c.268+72187G= MANE Select	NP_001020787.2:n.268+72187G=
NM_001042669.2:c.-18+15194G=	NP_001036134.1:n.-18+15194G=
NM_001346093.2:c.-104+15194G=	NP_001333022.1:n.-104+15194G=