Canonical Allele Identifier: CA101277277

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs929524796
• gnomAD v2: 4-86673986-G-GAGC
• gnomAD v3: 4-85752833-G-GAGC
• gnomAD v4: 4-85752833-G-GAGC
• MyVariant Identifiers: chr4:g.86673986_86673987insAGC (hg19) ; chr4:g.85752833_85752834insAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85752834_85752836dup , CM000666.2:g.85752834_85752836dup	GRCh38
NC_000004.11:g.86673987_86673989dup , CM000666.1:g.86673987_86673989dup	GRCh37
NC_000004.10:g.86893011_86893013dup	NCBI36
NG_051627.1:g.282704_282706dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+30862_268+30864dup MANE Select	ENSP00000378611.1:n.268+30862_268+30864dup
ENST00000395184.5:c.268+30862_268+30864dup	ENSP00000378611.1:n.268+30862_268+30864dup
ENST00000503995.5:c.268+30862_268+30864dup	ENSP00000423206.1:n.268+30862_268+30864dup
ENST00000512201.5:c.-18+30862_-18+30864dup	ENSP00000426105.1:n.-18+30862_-18+30864dup
NM_001025616.2:c.268+30862_268+30864dup	NP_001020787.2:n.268+30862_268+30864dup
XM_005263263.3:c.268+30862_268+30864dup	XP_005263320.1:n.268+30862_268+30864dup
XM_024454238.1:c.-18+30862_-18+30864dup	XP_024310006.1:n.-18+30862_-18+30864dup
XM_024454239.1:c.-18+30862_-18+30864dup	XP_024310007.1:n.-18+30862_-18+30864dup
NM_001025616.3:c.268+30862_268+30864dup MANE Select	NP_001020787.2:n.268+30862_268+30864dup