Canonical Allele Identifier: CA11783660

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs7687906
• gnomAD v2: 4-86715312-G-T
• gnomAD v3: 4-85794159-G-T
• gnomAD v4: 4-85794159-G-T
• MyVariant Identifiers: chr4:g.86715312G>T (hg19) ; chr4:g.85794159G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85794159G>T , CM000666.2:g.85794159G>T	GRCh38
NC_000004.11:g.86715312G>T , CM000666.1:g.86715312G>T	GRCh37
NC_000004.10:g.86934336G>T	NCBI36
NG_051627.1:g.324029G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395184.6:c.268+72187G>T MANE Select	ENSP00000378611.1:n.268+72187G>T
ENST00000395183.6:c.-18+15194G>T	ENSP00000378610.2:n.-18+15194G>T
ENST00000395184.5:c.268+72187G>T	ENSP00000378611.1:n.268+72187G>T
ENST00000503995.5:c.268+72187G>T	ENSP00000423206.1:n.268+72187G>T
ENST00000512201.5:c.-18+72187G>T	ENSP00000426105.1:n.-18+72187G>T
NM_001025616.2:c.268+72187G>T	NP_001020787.2:n.268+72187G>T
NM_001042669.1:c.-18+15194G>T	NP_001036134.1:n.-18+15194G>T
XM_005263263.3:c.268+72187G>T	XP_005263320.1:n.268+72187G>T
NM_001346093.1:c.-104+15194G>T	NP_001333022.1:n.-104+15194G>T
XM_024454238.1:c.-18+72187G>T	XP_024310006.1:n.-18+72187G>T
XM_024454239.1:c.-18+72187G>T	XP_024310007.1:n.-18+72187G>T
NM_001025616.3:c.268+72187G>T MANE Select	NP_001020787.2:n.268+72187G>T
NM_001042669.2:c.-18+15194G>T	NP_001036134.1:n.-18+15194G>T
NM_001346093.2:c.-104+15194G>T	NP_001333022.1:n.-104+15194G>T