Canonical Allele Identifier: CA2339183458
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056762106
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003924_47003925insAACA , CM000681.2:g.47003924_47003925insAACA GRCh38
NC_000019.9:g.47507181_47507182insAACA , CM000681.1:g.47507181_47507182insAACA GRCh37
NC_000019.8:g.52199021_52199022insAACA NCBI36
NG_047014.1:g.90358_90359insAACA
NG_047014.2:g.147928_147929insAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7736_7737insAACA ENSP00000385720.2:n.7736_7737insAACA
ENST00000672722.1:c.*3236_*3237insAACA MANE Select ENSP00000500409.1:n.*3236_*3237insAACA
ENST00000404338.7:c.7736_7737insAACA ENSP00000385720.2:n.7736_7737insAACA
ENST00000614079.1:c.7313_7314insAACA ENSP00000483730.1:n.7313_7314insAACA
NM_004491.4:c.7736_7737insAACA NP_004482.4:n.7736_7737insAACA
NM_004491.5:c.*3236_*3237insAACA MANE Select NP_004482.4:n.*3236_*3237insAACA
Search 100 bp 5'
Search 100 bp 3'