Canonical Allele Identifier: CA996445446
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056762389
gnomAD v3: 19-47003949-C-CAA
gnomAD v4: 19-47003949-C-CAA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003952_47003953dup , CM000681.2:g.47003952_47003953dup GRCh38
NC_000019.9:g.47507209_47507210dup , CM000681.1:g.47507209_47507210dup GRCh37
NC_000019.8:g.52199049_52199050dup NCBI36
NG_047014.1:g.90386_90387dup
NG_047014.2:g.147956_147957dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7764_7765dup ENSP00000385720.2:n.7764_7765dup
ENST00000672722.1:c.*3264_*3265dup MANE Select ENSP00000500409.1:n.*3264_*3265dup
ENST00000404338.7:c.7764_7765dup ENSP00000385720.2:n.7764_7765dup
ENST00000614079.1:c.7341_7342dup ENSP00000483730.1:n.7341_7342dup
NM_004491.4:c.7764_7765dup NP_004482.4:n.7764_7765dup
NM_004491.5:c.*3264_*3265dup MANE Select NP_004482.4:n.*3264_*3265dup
Search 100 bp 5'
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