Canonical Allele Identifier: CA2586003849

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47003953-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003954dup , CM000681.2:g.47003954dup	GRCh38
NC_000019.9:g.47507211dup , CM000681.1:g.47507211dup	GRCh37
NC_000019.8:g.52199051dup	NCBI36
NG_047014.1:g.90388dup
NG_047014.2:g.147958dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7766dup	ENSP00000385720.2:n.7766dup
ENST00000672722.1:c.*3266dup MANE Select	ENSP00000500409.1:n.*3266dup
ENST00000404338.7:c.7766dup	ENSP00000385720.2:n.7766dup
ENST00000614079.1:c.7343dup	ENSP00000483730.1:n.7343dup
NM_004491.4:c.7766dup	NP_004482.4:n.7766dup
NM_004491.5:c.*3266dup MANE Select	NP_004482.4:n.*3266dup