Canonical Allele Identifier: CA2586003742
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003900-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003902del , CM000681.2:g.47003902del GRCh38
NC_000019.9:g.47507159del , CM000681.1:g.47507159del GRCh37
NC_000019.8:g.52198999del NCBI36
NG_047014.1:g.90336del
NG_047014.2:g.147906del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7714del ENSP00000385720.2:n.7714del
ENST00000672722.1:c.*3214del MANE Select ENSP00000500409.1:n.*3214del
ENST00000404338.7:c.7714del ENSP00000385720.2:n.7714del
ENST00000614079.1:c.7291del ENSP00000483730.1:n.7291del
NM_004491.4:c.7714del NP_004482.4:n.7714del
NM_004491.5:c.*3214del MANE Select NP_004482.4:n.*3214del
Search 100 bp 5'
Search 100 bp 3'