Canonical Allele Identifier: CA799419772

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs1185837625
• gnomAD v3: 4-85753129-A-T
• gnomAD v4: 4-85753129-A-T
• MyVariant Identifiers: chr4:g.86674282A>T (hg19) ; chr4:g.85753129A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85753129A>T , CM000666.2:g.85753129A>T	GRCh38
NC_000004.11:g.86674282A>T , CM000666.1:g.86674282A>T	GRCh37
NC_000004.10:g.86893306A>T	NCBI36
NG_051627.1:g.282999A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395184.6:c.268+31157A>T MANE Select	ENSP00000378611.1:n.268+31157A>T
ENST00000395184.5:c.268+31157A>T	ENSP00000378611.1:n.268+31157A>T
ENST00000503995.5:c.268+31157A>T	ENSP00000423206.1:n.268+31157A>T
ENST00000512201.5:c.-18+31157A>T	ENSP00000426105.1:n.-18+31157A>T
NM_001025616.2:c.268+31157A>T	NP_001020787.2:n.268+31157A>T
XM_005263263.3:c.268+31157A>T	XP_005263320.1:n.268+31157A>T
XM_024454238.1:c.-18+31157A>T	XP_024310006.1:n.-18+31157A>T
XM_024454239.1:c.-18+31157A>T	XP_024310007.1:n.-18+31157A>T
NM_001025616.3:c.268+31157A>T MANE Select	NP_001020787.2:n.268+31157A>T