Canonical Allele Identifier: CA309123970
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs752133823
gnomAD v3: 19-47003913-GACACGCACAC-G
gnomAD v4: 19-47003913-GACACGCACAC-G
MyVariant Identifiers: chr19:g.47507171_47507180del (hg19) chr19:g.47003914_47003923del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003918_47003927del , CM000681.2:g.47003918_47003927del GRCh38
NC_000019.9:g.47507175_47507184del , CM000681.1:g.47507175_47507184del GRCh37
NC_000019.8:g.52199015_52199024del NCBI36
NG_047014.1:g.90352_90361del
NG_047014.2:g.147922_147931del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7730_7739del ENSP00000385720.2:n.7730_7739del
ENST00000672722.1:c.*3230_*3239del MANE Select ENSP00000500409.1:n.*3230_*3239del
ENST00000404338.7:c.7730_7739del ENSP00000385720.2:n.7730_7739del
ENST00000614079.1:c.7307_7316del ENSP00000483730.1:n.7307_7316del
NM_004491.4:c.7730_7739del NP_004482.4:n.7730_7739del
NM_004491.5:c.*3230_*3239del MANE Select NP_004482.4:n.*3230_*3239del
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