Canonical Allele Identifier: CA2339183739
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056765091
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004352_47004359del , CM000681.2:g.47004352_47004359del GRCh38
NC_000019.9:g.47507609_47507616del , CM000681.1:g.47507609_47507616del GRCh37
NC_000019.8:g.52199449_52199456del NCBI36
NG_047014.1:g.90786_90793del
NG_047014.2:g.148356_148363del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8164_8171del ENSP00000385720.2:n.8164_8171del
ENST00000672722.1:c.*3664_*3671del MANE Select ENSP00000500409.1:n.*3664_*3671del
ENST00000404338.7:c.8164_8171del ENSP00000385720.2:n.8164_8171del
NM_004491.4:c.8164_8171del NP_004482.4:n.8164_8171del
NM_004491.5:c.*3664_*3671del MANE Select NP_004482.4:n.*3664_*3671del
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