Canonical Allele Identifier: CA2586004219
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47004297-GGCGCGGCCGCGGTGCGGTCGGTGCAGCGTGGCCAAT-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004305_47004340del , CM000681.2:g.47004305_47004340del GRCh38
NC_000019.9:g.47507562_47507597del , CM000681.1:g.47507562_47507597del GRCh37
NC_000019.8:g.52199402_52199437del NCBI36
NG_047014.1:g.90739_90774del
NG_047014.2:g.148309_148344del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8117_8152del ENSP00000385720.2:n.8117_8152del
ENST00000672722.1:c.*3617_*3652del MANE Select ENSP00000500409.1:n.*3617_*3652del
ENST00000404338.7:c.8117_8152del ENSP00000385720.2:n.8117_8152del
NM_004491.4:c.8117_8152del NP_004482.4:n.8117_8152del
NM_004491.5:c.*3617_*3652del MANE Select NP_004482.4:n.*3617_*3652del
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