Canonical Allele Identifier: CA2586003764
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003912-G-GTA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003912_47003913insTA , CM000681.2:g.47003912_47003913insTA GRCh38
NC_000019.9:g.47507169_47507170insTA , CM000681.1:g.47507169_47507170insTA GRCh37
NC_000019.8:g.52199009_52199010insTA NCBI36
NG_047014.1:g.90346_90347insTA
NG_047014.2:g.147916_147917insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7724_7725insTA ENSP00000385720.2:n.7724_7725insTA
ENST00000672722.1:c.*3224_*3225insTA MANE Select ENSP00000500409.1:n.*3224_*3225insTA
ENST00000404338.7:c.7724_7725insTA ENSP00000385720.2:n.7724_7725insTA
ENST00000614079.1:c.7301_7302insTA ENSP00000483730.1:n.7301_7302insTA
NM_004491.4:c.7724_7725insTA NP_004482.4:n.7724_7725insTA
NM_004491.5:c.*3224_*3225insTA MANE Select NP_004482.4:n.*3224_*3225insTA
Search 100 bp 5'
Search 100 bp 3'