Canonical Allele Identifier: CA101277293

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs997462119
• gnomAD v3: 4-85753009-T-C
• gnomAD v4: 4-85753009-T-C
• MyVariant Identifiers: chr4:g.86674162T>C (hg19) ; chr4:g.85753009T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85753009T>C , CM000666.2:g.85753009T>C	GRCh38
NC_000004.11:g.86674162T>C , CM000666.1:g.86674162T>C	GRCh37
NC_000004.10:g.86893186T>C	NCBI36
NG_051627.1:g.282879T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395184.6:c.268+31037T>C MANE Select	ENSP00000378611.1:n.268+31037T>C
ENST00000395184.5:c.268+31037T>C	ENSP00000378611.1:n.268+31037T>C
ENST00000503995.5:c.268+31037T>C	ENSP00000423206.1:n.268+31037T>C
ENST00000512201.5:c.-18+31037T>C	ENSP00000426105.1:n.-18+31037T>C
NM_001025616.2:c.268+31037T>C	NP_001020787.2:n.268+31037T>C
XM_005263263.3:c.268+31037T>C	XP_005263320.1:n.268+31037T>C
XM_024454238.1:c.-18+31037T>C	XP_024310006.1:n.-18+31037T>C
XM_024454239.1:c.-18+31037T>C	XP_024310007.1:n.-18+31037T>C
NM_001025616.3:c.268+31037T>C MANE Select	NP_001020787.2:n.268+31037T>C