Canonical Allele Identifier: CA2814602914
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004351del , CM000681.2:g.47004351del GRCh38
NC_000019.9:g.47507608del , CM000681.1:g.47507608del GRCh37
NC_000019.8:g.52199448del NCBI36
NG_047014.1:g.90785del
NG_047014.2:g.148355del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8163del ENSP00000385720.2:n.8163del
ENST00000672722.1:c.*3663del MANE Select ENSP00000500409.1:n.*3663del
ENST00000404338.7:c.8163del ENSP00000385720.2:n.8163del
NM_004491.4:c.8163del NP_004482.4:n.8163del
NM_004491.5:c.*3663del MANE Select NP_004482.4:n.*3663del