Canonical Allele Identifier: CA2586003787

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47003924-A-ACG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003925_47003926insGC , CM000681.2:g.47003925_47003926insGC	GRCh38
NC_000019.9:g.47507182_47507183insGC , CM000681.1:g.47507182_47507183insGC	GRCh37
NC_000019.8:g.52199022_52199023insGC	NCBI36
NG_047014.1:g.90359_90360insGC
NG_047014.2:g.147929_147930insGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7737_7738insGC	ENSP00000385720.2:n.7737_7738insGC
ENST00000672722.1:c.*3237_*3238insGC MANE Select	ENSP00000500409.1:n.*3237_*3238insGC
ENST00000404338.7:c.7737_7738insGC	ENSP00000385720.2:n.7737_7738insGC
ENST00000614079.1:c.7314_7315insGC	ENSP00000483730.1:n.7314_7315insGC
NM_004491.4:c.7737_7738insGC	NP_004482.4:n.7737_7738insGC
NM_004491.5:c.*3237_*3238insGC MANE Select	NP_004482.4:n.*3237_*3238insGC