Canonical Allele Identifier: CA2586003810
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003938-A-ACACT
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003941_47003942insTCAC , CM000681.2:g.47003941_47003942insTCAC GRCh38
NC_000019.9:g.47507198_47507199insTCAC , CM000681.1:g.47507198_47507199insTCAC GRCh37
NC_000019.8:g.52199038_52199039insTCAC NCBI36
NG_047014.1:g.90375_90376insTCAC
NG_047014.2:g.147945_147946insTCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7753_7754insTCAC ENSP00000385720.2:n.7753_7754insTCAC
ENST00000672722.1:c.*3253_*3254insTCAC MANE Select ENSP00000500409.1:n.*3253_*3254insTCAC
ENST00000404338.7:c.7753_7754insTCAC ENSP00000385720.2:n.7753_7754insTCAC
ENST00000614079.1:c.7330_7331insTCAC ENSP00000483730.1:n.7330_7331insTCAC
NM_004491.4:c.7753_7754insTCAC NP_004482.4:n.7753_7754insTCAC
NM_004491.5:c.*3253_*3254insTCAC MANE Select NP_004482.4:n.*3253_*3254insTCAC
Search 100 bp 5'
Search 100 bp 3'