Canonical Allele Identifier: CA2586004312
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47004391-CCTGGGCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004392_47004398del , CM000681.2:g.47004392_47004398del GRCh38
NC_000019.9:g.47507649_47507655del , CM000681.1:g.47507649_47507655del GRCh37
NC_000019.8:g.52199489_52199495del NCBI36
NG_047014.1:g.90826_90832del
NG_047014.2:g.148396_148402del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8204_8210del ENSP00000385720.2:n.8204_8210del
ENST00000672722.1:c.*3704_*3710del MANE Select ENSP00000500409.1:n.*3704_*3710del
ENST00000404338.7:c.8204_8210del ENSP00000385720.2:n.8204_8210del
NM_004491.4:c.8204_8210del NP_004482.4:n.8204_8210del
NM_004491.5:c.*3704_*3710del MANE Select NP_004482.4:n.*3704_*3710del
Search 100 bp 5'
Search 100 bp 3'