Canonical Allele Identifier: CA1473771644

Gene: ARHGAP24

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85719996A= , CM000666.2:g.85719996A=	GRCh38
NC_000004.11:g.86641149A= , CM000666.1:g.86641149A=	GRCh37
NC_000004.10:g.86860173A=	NCBI36
NG_051627.1:g.249866A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001025616.3:c.181-1889A= MANE Select	NP_001020787.2:n.181-1889A=
ENST00000395184.6:c.181-1889A= MANE Select	ENSP00000378611.1:n.181-1889A=
NM_001025616.2:c.181-1889A=	NP_001020787.2:n.181-1889A=
ENST00000395184.5:c.181-1889A=	ENSP00000378611.1:n.181-1889A=
ENST00000503995.5:c.181-1889A=	ENSP00000423206.1:n.181-1889A=
ENST00000506421.5:n.318-1889A=
ENST00000509709.1:n.130-1889A=
ENST00000512201.5:c.-105-1889A=	ENSP00000426105.1:n.-105-1889A=
XM_005263263.3:c.181-1889A=	XP_005263320.1:n.181-1889A=
XM_024454238.1:c.-105-1889A=	XP_024310006.1:n.-105-1889A=
XM_024454239.1:c.-105-1889A=	XP_024310007.1:n.-105-1889A=