Canonical Allele Identifier: CA2339183443

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003917_47003918delinsCG , CM000681.2:g.47003917_47003918delinsCG	GRCh38
NC_000019.9:g.47507174_47507175delinsCG , CM000681.1:g.47507174_47507175delinsCG	GRCh37
NC_000019.8:g.52199014_52199015delinsCG	NCBI36
NG_047014.1:g.90351_90352delinsCG
NG_047014.2:g.147921_147922delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7729_7730delinsCG	ENSP00000385720.2:n.7729_7730delinsCG
ENST00000672722.1:c.*3229_*3230delinsCG MANE Select	ENSP00000500409.1:n.*3229_*3230delinsCG
ENST00000404338.7:c.7729_7730delinsCG	ENSP00000385720.2:n.7729_7730delinsCG
ENST00000614079.1:c.7306_7307delinsCG	ENSP00000483730.1:n.7306_7307delinsCG
NM_004491.4:c.7729_7730delinsCG	NP_004482.4:n.7729_7730delinsCG
NM_004491.5:c.*3229_*3230delinsCG MANE Select	NP_004482.4:n.*3229_*3230delinsCG