Canonical Allele Identifier: CA2586003640
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003824-ACTCAGCTCC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003825_47003833del , CM000681.2:g.47003825_47003833del GRCh38
NC_000019.9:g.47507082_47507090del , CM000681.1:g.47507082_47507090del GRCh37
NC_000019.8:g.52198922_52198930del NCBI36
NG_047014.1:g.90259_90267del
NG_047014.2:g.147829_147837del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7637_7645del ENSP00000385720.2:n.7637_7645del
ENST00000672722.1:c.*3137_*3145del MANE Select ENSP00000500409.1:n.*3137_*3145del
ENST00000404338.7:c.7637_7645del ENSP00000385720.2:n.7637_7645del
ENST00000614079.1:c.7214_7222del ENSP00000483730.1:n.7214_7222del
NM_004491.4:c.7637_7645del NP_004482.4:n.7637_7645del
NM_004491.5:c.*3137_*3145del MANE Select NP_004482.4:n.*3137_*3145del
Search 100 bp 5'
Search 100 bp 3'