Canonical Allele Identifier: CA882866589
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs375875258
gnomAD v3: 19-47003913-G-GACACACACAC
gnomAD v4: 19-47003913-G-GACACACACAC
MyVariant Identifiers: chr19:g.47507170_47507171insACACACACAC (hg19) chr19:g.47003913_47003914insACACACACAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003917_47003918insACACACACAC , CM000681.2:g.47003917_47003918insACACACACAC GRCh38
NC_000019.9:g.47507174_47507175insACACACACAC , CM000681.1:g.47507174_47507175insACACACACAC GRCh37
NC_000019.8:g.52199014_52199015insACACACACAC NCBI36
NG_047014.1:g.90351_90352insACACACACAC
NG_047014.2:g.147921_147922insACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7729_7730insACACACACAC ENSP00000385720.2:n.7729_7730insACACACACAC
ENST00000672722.1:c.*3229_*3230insACACACACAC MANE Select ENSP00000500409.1:n.*3229_*3230insACACACACAC
ENST00000404338.7:c.7729_7730insACACACACAC ENSP00000385720.2:n.7729_7730insACACACACAC
ENST00000614079.1:c.7306_7307insACACACACAC ENSP00000483730.1:n.7306_7307insACACACACAC
NM_004491.4:c.7729_7730insACACACACAC NP_004482.4:n.7729_7730insACACACACAC
NM_004491.5:c.*3229_*3230insACACACACAC MANE Select NP_004482.4:n.*3229_*3230insACACACACAC
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