Canonical Allele Identifier: CA633401860
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs375875258
gnomAD v2: 19-47507170-G-GACACACAC
gnomAD v3: 19-47003913-G-GACACACAC
gnomAD v4: 19-47003913-G-GACACACAC
MyVariant Identifiers: chr19:g.47507175_47507178delinsACACACACGCAC (hg19) chr19:g.47507170_47507171insACACACAC (hg19) chr19:g.47003918_47003921delinsACACACACGCAC (hg38) chr19:g.47003913_47003914insACACACAC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003917_47003918insACACACAC , CM000681.2:g.47003917_47003918insACACACAC GRCh38
NC_000019.9:g.47507174_47507175insACACACAC , CM000681.1:g.47507174_47507175insACACACAC GRCh37
NC_000019.8:g.52199014_52199015insACACACAC NCBI36
NG_047014.1:g.90351_90352insACACACAC
NG_047014.2:g.147921_147922insACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7729_7730insACACACAC ENSP00000385720.2:n.7729_7730insACACACAC
ENST00000672722.1:c.*3229_*3230insACACACAC MANE Select ENSP00000500409.1:n.*3229_*3230insACACACAC
ENST00000404338.7:c.7729_7730insACACACAC ENSP00000385720.2:n.7729_7730insACACACAC
ENST00000614079.1:c.7306_7307insACACACAC ENSP00000483730.1:n.7306_7307insACACACAC
NM_004491.4:c.7729_7730insACACACAC NP_004482.4:n.7729_7730insACACACAC
NM_004491.5:c.*3229_*3230insACACACAC MANE Select NP_004482.4:n.*3229_*3230insACACACAC
Search 100 bp 5'
Search 100 bp 3'