Canonical Allele Identifier: CA2339183697
Gene: ARHGAP35 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004305C= , CM000681.2:g.47004305C= GRCh38
NC_000019.9:g.47507562C= , CM000681.1:g.47507562C= GRCh37
NC_000019.8:g.52199402C= NCBI36
NG_047014.1:g.90739C=
NG_047014.2:g.148309C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8117C= ENSP00000385720.2:n.8117C=
ENST00000672722.1:c.*3617C= MANE Select ENSP00000500409.1:n.*3617C=
ENST00000404338.7:c.8117C= ENSP00000385720.2:n.8117C=
ENST00000614079.1:c.7694C= ENSP00000483730.1:n.7694C=
NM_004491.4:c.8117C= NP_004482.4:n.8117C=
NM_004491.5:c.*3617C= MANE Select NP_004482.4:n.*3617C=
Search 100 bp 5'
Search 100 bp 3'