Canonical Allele Identifier: CA1064979706

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs1726314361
• gnomAD v3: 4-85752838-C-T
• gnomAD v4: 4-85752838-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85752838C>T , CM000666.2:g.85752838C>T	GRCh38
NC_000004.11:g.86673991C>T , CM000666.1:g.86673991C>T	GRCh37
NC_000004.10:g.86893015C>T	NCBI36
NG_051627.1:g.282708C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+30866C>T MANE Select	ENSP00000378611.1:n.268+30866C>T
ENST00000395184.5:c.268+30866C>T	ENSP00000378611.1:n.268+30866C>T
ENST00000503995.5:c.268+30866C>T	ENSP00000423206.1:n.268+30866C>T
ENST00000512201.5:c.-18+30866C>T	ENSP00000426105.1:n.-18+30866C>T
NM_001025616.2:c.268+30866C>T	NP_001020787.2:n.268+30866C>T
XM_005263263.3:c.268+30866C>T	XP_005263320.1:n.268+30866C>T
XM_024454238.1:c.-18+30866C>T	XP_024310006.1:n.-18+30866C>T
XM_024454239.1:c.-18+30866C>T	XP_024310007.1:n.-18+30866C>T
NM_001025616.3:c.268+30866C>T MANE Select	NP_001020787.2:n.268+30866C>T