Canonical Allele Identifier: CA2586003770
Gene: ARHGAP35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003918_47003937del , CM000681.2:g.47003918_47003937del GRCh38
NC_000019.9:g.47507175_47507194del , CM000681.1:g.47507175_47507194del GRCh37
NC_000019.8:g.52199015_52199034del NCBI36
NG_047014.1:g.90352_90371del
NG_047014.2:g.147922_147941del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7730_7749del ENSP00000385720.2:n.7730_7749del
ENST00000672722.1:c.*3230_*3249del MANE Select ENSP00000500409.1:n.*3230_*3249del
ENST00000404338.7:c.7730_7749del ENSP00000385720.2:n.7730_7749del
ENST00000614079.1:c.7307_7326del ENSP00000483730.1:n.7307_7326del
NM_004491.4:c.7730_7749del NP_004482.4:n.7730_7749del
NM_004491.5:c.*3230_*3249del MANE Select NP_004482.4:n.*3230_*3249del