Canonical Allele Identifier: CA996445465
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1408493618
gnomAD v3: 19-47004338-GGC-G
gnomAD v4: 19-47004338-GGC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004346_47004347del , CM000681.2:g.47004346_47004347del GRCh38
NC_000019.9:g.47507603_47507604del , CM000681.1:g.47507603_47507604del GRCh37
NC_000019.8:g.52199443_52199444del NCBI36
NG_047014.1:g.90780_90781del
NG_047014.2:g.148350_148351del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8158_8159del ENSP00000385720.2:n.8158_8159del
ENST00000672722.1:c.*3658_*3659del MANE Select ENSP00000500409.1:n.*3658_*3659del
ENST00000404338.7:c.8158_8159del ENSP00000385720.2:n.8158_8159del
NM_004491.4:c.8158_8159del NP_004482.4:n.8158_8159del
NM_004491.5:c.*3658_*3659del MANE Select NP_004482.4:n.*3658_*3659del
Search 100 bp 5'
Search 100 bp 3'