Canonical Allele Identifier: CA920121805
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs869040892
gnomAD v4: 19-47003918-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003919del , CM000681.2:g.47003919del GRCh38
NC_000019.9:g.47507176del , CM000681.1:g.47507176del GRCh37
NC_000019.8:g.52199016del NCBI36
NG_047014.1:g.90353del
NG_047014.2:g.147923del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7731del ENSP00000385720.2:n.7731del
ENST00000672722.1:c.*3231del MANE Select ENSP00000500409.1:n.*3231del
ENST00000404338.7:c.7731del ENSP00000385720.2:n.7731del
ENST00000614079.1:c.7308del ENSP00000483730.1:n.7308del
NM_004491.4:c.7731del NP_004482.4:n.7731del
NM_004491.5:c.*3231del MANE Select NP_004482.4:n.*3231del
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Search 100 bp 3'