Canonical Allele Identifier: CA2339183725
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004338_47004340delinsGGC , CM000681.2:g.47004338_47004340delinsGGC GRCh38
NC_000019.9:g.47507595_47507597delinsGGC , CM000681.1:g.47507595_47507597delinsGGC GRCh37
NC_000019.8:g.52199435_52199437delinsGGC NCBI36
NG_047014.1:g.90772_90774delinsGGC
NG_047014.2:g.148342_148344delinsGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8150_8152delinsGGC ENSP00000385720.2:n.8150_8152delinsGGC
ENST00000672722.1:c.*3650_*3652delinsGGC MANE Select ENSP00000500409.1:n.*3650_*3652delinsGGC
ENST00000404338.7:c.8150_8152delinsGGC ENSP00000385720.2:n.8150_8152delinsGGC
NM_004491.4:c.8150_8152delinsGGC NP_004482.4:n.8150_8152delinsGGC
NM_004491.5:c.*3650_*3652delinsGGC MANE Select NP_004482.4:n.*3650_*3652delinsGGC