Canonical Allele Identifier: CA2586003772
Gene: ARHGAP35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003917_47003918insTCACACAC , CM000681.2:g.47003917_47003918insTCACACAC GRCh38
NC_000019.9:g.47507174_47507175insTCACACAC , CM000681.1:g.47507174_47507175insTCACACAC GRCh37
NC_000019.8:g.52199014_52199015insTCACACAC NCBI36
NG_047014.1:g.90351_90352insTCACACAC
NG_047014.2:g.147921_147922insTCACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7729_7730insTCACACAC ENSP00000385720.2:n.7729_7730insTCACACAC
ENST00000672722.1:c.*3229_*3230insTCACACAC MANE Select ENSP00000500409.1:n.*3229_*3230insTCACACAC
ENST00000404338.7:c.7729_7730insTCACACAC ENSP00000385720.2:n.7729_7730insTCACACAC
ENST00000614079.1:c.7306_7307insTCACACAC ENSP00000483730.1:n.7306_7307insTCACACAC
NM_004491.4:c.7729_7730insTCACACAC NP_004482.4:n.7729_7730insTCACACAC
NM_004491.5:c.*3229_*3230insTCACACAC MANE Select NP_004482.4:n.*3229_*3230insTCACACAC