Canonical Allele Identifier: CA2339183702
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056764708

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004309del , CM000681.2:g.47004309del GRCh38
NC_000019.9:g.47507566del , CM000681.1:g.47507566del GRCh37
NC_000019.8:g.52199406del NCBI36
NG_047014.1:g.90743del
NG_047014.2:g.148313del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8121del ENSP00000385720.2:n.8121del
ENST00000672722.1:c.*3621del MANE Select ENSP00000500409.1:n.*3621del
ENST00000404338.7:c.8121del ENSP00000385720.2:n.8121del
NM_004491.4:c.8121del NP_004482.4:n.8121del
NM_004491.5:c.*3621del MANE Select NP_004482.4:n.*3621del