Canonical Allele Identifier: CA2586003699

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47003879-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003881del , CM000681.2:g.47003881del	GRCh38
NC_000019.9:g.47507138del , CM000681.1:g.47507138del	GRCh37
NC_000019.8:g.52198978del	NCBI36
NG_047014.1:g.90315del
NG_047014.2:g.147885del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7693del	ENSP00000385720.2:n.7693del
ENST00000672722.1:c.*3193del MANE Select	ENSP00000500409.1:n.*3193del
ENST00000404338.7:c.7693del	ENSP00000385720.2:n.7693del
ENST00000614079.1:c.7270del	ENSP00000483730.1:n.7270del
NM_004491.4:c.7693del	NP_004482.4:n.7693del
NM_004491.5:c.*3193del MANE Select	NP_004482.4:n.*3193del