Canonical Allele Identifier: CA2339183413
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003875C= , CM000681.2:g.47003875C= GRCh38
NC_000019.9:g.47507132C= , CM000681.1:g.47507132C= GRCh37
NC_000019.8:g.52198972C= NCBI36
NG_047014.1:g.90309C=
NG_047014.2:g.147879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7687C= ENSP00000385720.2:n.7687C=
ENST00000672722.1:c.*3187C= MANE Select ENSP00000500409.1:n.*3187C=
ENST00000404338.7:c.7687C= ENSP00000385720.2:n.7687C=
ENST00000614079.1:c.7264C= ENSP00000483730.1:n.7264C=
NM_004491.4:c.7687C= NP_004482.4:n.7687C=
NM_004491.5:c.*3187C= MANE Select NP_004482.4:n.*3187C=