Canonical Allele Identifier: CA2586003847

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47003952-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003952_47003953insG , CM000681.2:g.47003952_47003953insG	GRCh38
NC_000019.9:g.47507209_47507210insG , CM000681.1:g.47507209_47507210insG	GRCh37
NC_000019.8:g.52199049_52199050insG	NCBI36
NG_047014.1:g.90386_90387insG
NG_047014.2:g.147956_147957insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7764_7765insG	ENSP00000385720.2:n.7764_7765insG
ENST00000672722.1:c.*3264_*3265insG MANE Select	ENSP00000500409.1:n.*3264_*3265insG
ENST00000404338.7:c.7764_7765insG	ENSP00000385720.2:n.7764_7765insG
ENST00000614079.1:c.7341_7342insG	ENSP00000483730.1:n.7341_7342insG
NM_004491.4:c.7764_7765insG	NP_004482.4:n.7764_7765insG
NM_004491.5:c.*3264_*3265insG MANE Select	NP_004482.4:n.*3264_*3265insG