Canonical Allele Identifier: CA2735909688
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1555768186
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003917_47003918insACCC , CM000681.2:g.47003917_47003918insACCC GRCh38
NC_000019.9:g.47507174_47507175insACCC , CM000681.1:g.47507174_47507175insACCC GRCh37
NC_000019.8:g.52199014_52199015insACCC NCBI36
NG_047014.1:g.90351_90352insACCC
NG_047014.2:g.147921_147922insACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7729_7730insACCC ENSP00000385720.2:n.7729_7730insACCC
ENST00000672722.1:c.*3229_*3230insACCC MANE Select ENSP00000500409.1:n.*3229_*3230insACCC
ENST00000404338.7:c.7729_7730insACCC ENSP00000385720.2:n.7729_7730insACCC
ENST00000614079.1:c.7306_7307insACCC ENSP00000483730.1:n.7306_7307insACCC
NM_004491.4:c.7729_7730insACCC NP_004482.4:n.7729_7730insACCC
NM_004491.5:c.*3229_*3230insACCC MANE Select NP_004482.4:n.*3229_*3230insACCC
Search 100 bp 5'
Search 100 bp 3'