Canonical Allele Identifier: CA2586003840

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47003950-A-ACACG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003950_47003951insCACG , CM000681.2:g.47003950_47003951insCACG	GRCh38
NC_000019.9:g.47507207_47507208insCACG , CM000681.1:g.47507207_47507208insCACG	GRCh37
NC_000019.8:g.52199047_52199048insCACG	NCBI36
NG_047014.1:g.90384_90385insCACG
NG_047014.2:g.147954_147955insCACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7762_7763insCACG	ENSP00000385720.2:n.7762_7763insCACG
ENST00000672722.1:c.*3262_*3263insCACG MANE Select	ENSP00000500409.1:n.*3262_*3263insCACG
ENST00000404338.7:c.7762_7763insCACG	ENSP00000385720.2:n.7762_7763insCACG
ENST00000614079.1:c.7339_7340insCACG	ENSP00000483730.1:n.7339_7340insCACG
NM_004491.4:c.7762_7763insCACG	NP_004482.4:n.7762_7763insCACG
NM_004491.5:c.*3262_*3263insCACG MANE Select	NP_004482.4:n.*3262_*3263insCACG