Canonical Allele Identifier: CA2814602915
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004354_47004355insAT , CM000681.2:g.47004354_47004355insAT GRCh38
NC_000019.9:g.47507611_47507612insAT , CM000681.1:g.47507611_47507612insAT GRCh37
NC_000019.8:g.52199451_52199452insAT NCBI36
NG_047014.1:g.90788_90789insAT
NG_047014.2:g.148358_148359insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8166_8167insAT ENSP00000385720.2:n.8166_8167insAT
ENST00000672722.1:c.*3666_*3667insAT MANE Select ENSP00000500409.1:n.*3666_*3667insAT
ENST00000404338.7:c.8166_8167insAT ENSP00000385720.2:n.8166_8167insAT
NM_004491.4:c.8166_8167insAT NP_004482.4:n.8166_8167insAT
NM_004491.5:c.*3666_*3667insAT MANE Select NP_004482.4:n.*3666_*3667insAT