Canonical Allele Identifier: CA2586004296
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47004377-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004378del , CM000681.2:g.47004378del GRCh38
NC_000019.9:g.47507635del , CM000681.1:g.47507635del GRCh37
NC_000019.8:g.52199475del NCBI36
NG_047014.1:g.90812del
NG_047014.2:g.148382del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8190del ENSP00000385720.2:n.8190del
ENST00000672722.1:c.*3690del MANE Select ENSP00000500409.1:n.*3690del
ENST00000404338.7:c.8190del ENSP00000385720.2:n.8190del
NM_004491.4:c.8190del NP_004482.4:n.8190del
NM_004491.5:c.*3690del MANE Select NP_004482.4:n.*3690del
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