Canonical Allele Identifier: CA996445447
Gene: ARHGAP35 HGNC NCBI

Linked Data

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

HGVS Genome Assembly
NC_000019.10:g.47003953del , CM000681.2:g.47003953del GRCh38
NC_000019.9:g.47507210del , CM000681.1:g.47507210del GRCh37
NC_000019.8:g.52199050del NCBI36
NG_047014.1:g.90387del
NG_047014.2:g.147957del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7765del ENSP00000385720.2:n.7765del
ENST00000672722.1:c.*3265del MANE Select ENSP00000500409.1:n.*3265del
ENST00000404338.7:c.7765del ENSP00000385720.2:n.7765del
ENST00000614079.1:c.7342del ENSP00000483730.1:n.7342del
NM_004491.4:c.7765del NP_004482.4:n.7765del
NM_004491.5:c.*3265del MANE Select NP_004482.4:n.*3265del
Search 100 bp 5'
Search 100 bp 3'