Canonical Allele Identifier: CA2339183729
Gene: ARHGAP35 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004343G= , CM000681.2:g.47004343G= GRCh38
NC_000019.9:g.47507600G= , CM000681.1:g.47507600G= GRCh37
NC_000019.8:g.52199440G= NCBI36
NG_047014.1:g.90777G=
NG_047014.2:g.148347G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8155G= ENSP00000385720.2:n.8155G=
ENST00000672722.1:c.*3655G= MANE Select ENSP00000500409.1:n.*3655G=
ENST00000404338.7:c.8155G= ENSP00000385720.2:n.8155G=
NM_004491.4:c.8155G= NP_004482.4:n.8155G=
NM_004491.5:c.*3655G= MANE Select NP_004482.4:n.*3655G=
Search 100 bp 5'
Search 100 bp 3'