Canonical Allele Identifier: CA2586004214
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47004293-TG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004298del , CM000681.2:g.47004298del GRCh38
NC_000019.9:g.47507555del , CM000681.1:g.47507555del GRCh37
NC_000019.8:g.52199395del NCBI36
NG_047014.1:g.90732del
NG_047014.2:g.148302del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8110del ENSP00000385720.2:n.8110del
ENST00000672722.1:c.*3610del MANE Select ENSP00000500409.1:n.*3610del
ENST00000404338.7:c.8110del ENSP00000385720.2:n.8110del
ENST00000614079.1:c.7687del ENSP00000483730.1:n.7687del
NM_004491.4:c.8110del NP_004482.4:n.8110del
NM_004491.5:c.*3610del MANE Select NP_004482.4:n.*3610del
Search 100 bp 5'
Search 100 bp 3'