Canonical Allele Identifier: CA2586003794
Gene: ARHGAP35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003930_47003931insTACA , CM000681.2:g.47003930_47003931insTACA GRCh38
NC_000019.9:g.47507187_47507188insTACA , CM000681.1:g.47507187_47507188insTACA GRCh37
NC_000019.8:g.52199027_52199028insTACA NCBI36
NG_047014.1:g.90364_90365insTACA
NG_047014.2:g.147934_147935insTACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7742_7743insTACA ENSP00000385720.2:n.7742_7743insTACA
ENST00000672722.1:c.*3242_*3243insTACA MANE Select ENSP00000500409.1:n.*3242_*3243insTACA
ENST00000404338.7:c.7742_7743insTACA ENSP00000385720.2:n.7742_7743insTACA
ENST00000614079.1:c.7319_7320insTACA ENSP00000483730.1:n.7319_7320insTACA
NM_004491.4:c.7742_7743insTACA NP_004482.4:n.7742_7743insTACA
NM_004491.5:c.*3242_*3243insTACA MANE Select NP_004482.4:n.*3242_*3243insTACA