Canonical Allele Identifier: CA101274892

Gene: ARHGAP24

Linked Data

• dbSNP Id: rs1054395110
• gnomAD v3: 4-85730318-C-T
• gnomAD v4: 4-85730318-C-T
• MyVariant Identifiers: chr4:g.86651471C>T (hg19) ; chr4:g.85730318C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.85730318C>T , CM000666.2:g.85730318C>T	GRCh38
NC_000004.11:g.86651471C>T , CM000666.1:g.86651471C>T	GRCh37
NC_000004.10:g.86870495C>T	NCBI36
NG_051627.1:g.260188C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395184.6:c.268+8346C>T MANE Select	ENSP00000378611.1:n.268+8346C>T
ENST00000395184.5:c.268+8346C>T	ENSP00000378611.1:n.268+8346C>T
ENST00000503995.5:c.268+8346C>T	ENSP00000423206.1:n.268+8346C>T
ENST00000512201.5:c.-18+8346C>T	ENSP00000426105.1:n.-18+8346C>T
NM_001025616.2:c.268+8346C>T	NP_001020787.2:n.268+8346C>T
XM_005263263.3:c.268+8346C>T	XP_005263320.1:n.268+8346C>T
XM_024454238.1:c.-18+8346C>T	XP_024310006.1:n.-18+8346C>T
XM_024454239.1:c.-18+8346C>T	XP_024310007.1:n.-18+8346C>T
NM_001025616.3:c.268+8346C>T MANE Select	NP_001020787.2:n.268+8346C>T