Canonical Allele Identifier: CA799409632

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs1407947911
• MyVariant Identifiers: chr4:g.86651406T>A (hg19) ; chr4:g.85730253T>A (hg38)

Genomic Alleles

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

Transcript Alleles

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