Canonical Allele Identifier: CA2814602892
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003844del , CM000681.2:g.47003844del GRCh38
NC_000019.9:g.47507101del , CM000681.1:g.47507101del GRCh37
NC_000019.8:g.52198941del NCBI36
NG_047014.1:g.90278del
NG_047014.2:g.147848del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7656del ENSP00000385720.2:n.7656del
ENST00000672722.1:c.*3156del MANE Select ENSP00000500409.1:n.*3156del
ENST00000404338.7:c.7656del ENSP00000385720.2:n.7656del
ENST00000614079.1:c.7233del ENSP00000483730.1:n.7233del
NM_004491.4:c.7656del NP_004482.4:n.7656del
NM_004491.5:c.*3156del MANE Select NP_004482.4:n.*3156del