Canonical Allele Identifier: CA2339183695
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056764651
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004301del , CM000681.2:g.47004301del GRCh38
NC_000019.9:g.47507558del , CM000681.1:g.47507558del GRCh37
NC_000019.8:g.52199398del NCBI36
NG_047014.1:g.90735del
NG_047014.2:g.148305del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8113del ENSP00000385720.2:n.8113del
ENST00000672722.1:c.*3613del MANE Select ENSP00000500409.1:n.*3613del
ENST00000404338.7:c.8113del ENSP00000385720.2:n.8113del
ENST00000614079.1:c.7690del ENSP00000483730.1:n.7690del
NM_004491.4:c.8113del NP_004482.4:n.8113del
NM_004491.5:c.*3613del MANE Select NP_004482.4:n.*3613del
Search 100 bp 5'
Search 100 bp 3'