Canonical Allele Identifier: CA2586003929
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47004034-GCCACTGCTTT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004035_47004044del , CM000681.2:g.47004035_47004044del GRCh38
NC_000019.9:g.47507292_47507301del , CM000681.1:g.47507292_47507301del GRCh37
NC_000019.8:g.52199132_52199141del NCBI36
NG_047014.1:g.90469_90478del
NG_047014.2:g.148039_148048del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7847_7856del ENSP00000385720.2:n.7847_7856del
ENST00000672722.1:c.*3347_*3356del MANE Select ENSP00000500409.1:n.*3347_*3356del
ENST00000404338.7:c.7847_7856del ENSP00000385720.2:n.7847_7856del
ENST00000614079.1:c.7424_7433del ENSP00000483730.1:n.7424_7433del
NM_004491.4:c.7847_7856del NP_004482.4:n.7847_7856del
NM_004491.5:c.*3347_*3356del MANE Select NP_004482.4:n.*3347_*3356del
Search 100 bp 5'
Search 100 bp 3'