Canonical Allele Identifier: CA2814602917
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004358_47004359insGGCGCGCGCGGGG , CM000681.2:g.47004358_47004359insGGCGCGCGCGGGG GRCh38
NC_000019.9:g.47507615_47507616insGGCGCGCGCGGGG , CM000681.1:g.47507615_47507616insGGCGCGCGCGGGG GRCh37
NC_000019.8:g.52199455_52199456insGGCGCGCGCGGGG NCBI36
NG_047014.1:g.90792_90793insGGCGCGCGCGGGG
NG_047014.2:g.148362_148363insGGCGCGCGCGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8170_8171insGGCGCGCGCGGGG ENSP00000385720.2:n.8170_8171insGGCGCGCGCGGGG
ENST00000672722.1:c.*3670_*3671insGGCGCGCGCGGGG MANE Select ENSP00000500409.1:n.*3670_*3671insGGCGCGCGCGGGG
ENST00000404338.7:c.8170_8171insGGCGCGCGCGGGG ENSP00000385720.2:n.8170_8171insGGCGCGCGCGGGG
NM_004491.4:c.8170_8171insGGCGCGCGCGGGG NP_004482.4:n.8170_8171insGGCGCGCGCGGGG
NM_004491.5:c.*3670_*3671insGGCGCGCGCGGGG MANE Select NP_004482.4:n.*3670_*3671insGGCGCGCGCGGGG