Canonical Allele Identifier: CA406504826
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs35048370
gnomAD v2: 19-47507175-G-GCA
gnomAD v3: 19-47003918-G-GCA
gnomAD v4: 19-47003918-G-GCA
MyVariant Identifiers: chr19:g.47507177_47507178insCA (hg19) chr19:g.47507175_47507176insCA (hg19) chr19:g.47003920_47003921insCA (hg38) chr19:g.47003918_47003919insCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003949_47003950dup , CM000681.2:g.47003949_47003950dup GRCh38
NC_000019.9:g.47507206_47507207dup , CM000681.1:g.47507206_47507207dup GRCh37
NC_000019.8:g.52199046_52199047dup NCBI36
NG_047014.1:g.90383_90384dup
NG_047014.2:g.147953_147954dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7761_7762dup ENSP00000385720.2:n.7761_7762dup
ENST00000672722.1:c.*3261_*3262dup MANE Select ENSP00000500409.1:n.*3261_*3262dup
ENST00000404338.7:c.7761_7762dup ENSP00000385720.2:n.7761_7762dup
ENST00000614079.1:c.7338_7339dup ENSP00000483730.1:n.7338_7339dup
NM_004491.4:c.7761_7762dup NP_004482.4:n.7761_7762dup
NM_004491.5:c.*3261_*3262dup MANE Select NP_004482.4:n.*3261_*3262dup
Search 100 bp 5'
Search 100 bp 3'