Canonical Allele Identifier: CA553019299

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs1170721026
• gnomAD v2: 4-86673988-G-T
• gnomAD v3: 4-85752835-G-T
• gnomAD v4: 4-85752835-G-T
• MyVariant Identifiers: chr4:g.86673988G>T (hg19) ; chr4:g.85752835G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85752835G>T , CM000666.2:g.85752835G>T	GRCh38
NC_000004.11:g.86673988G>T , CM000666.1:g.86673988G>T	GRCh37
NC_000004.10:g.86893012G>T	NCBI36
NG_051627.1:g.282705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395184.6:c.268+30863G>T MANE Select	ENSP00000378611.1:n.268+30863G>T
ENST00000395184.5:c.268+30863G>T	ENSP00000378611.1:n.268+30863G>T
ENST00000503995.5:c.268+30863G>T	ENSP00000423206.1:n.268+30863G>T
ENST00000512201.5:c.-18+30863G>T	ENSP00000426105.1:n.-18+30863G>T
NM_001025616.2:c.268+30863G>T	NP_001020787.2:n.268+30863G>T
XM_005263263.3:c.268+30863G>T	XP_005263320.1:n.268+30863G>T
XM_024454238.1:c.-18+30863G>T	XP_024310006.1:n.-18+30863G>T
XM_024454239.1:c.-18+30863G>T	XP_024310007.1:n.-18+30863G>T
NM_001025616.3:c.268+30863G>T MANE Select	NP_001020787.2:n.268+30863G>T