Canonical Allele Identifier: CA2339183718
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004333T= , CM000681.2:g.47004333T= GRCh38
NC_000019.9:g.47507590T= , CM000681.1:g.47507590T= GRCh37
NC_000019.8:g.52199430T= NCBI36
NG_047014.1:g.90767T=
NG_047014.2:g.148337T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8145T= ENSP00000385720.2:n.8145T=
ENST00000672722.1:c.*3645T= MANE Select ENSP00000500409.1:n.*3645T=
ENST00000404338.7:c.8145T= ENSP00000385720.2:n.8145T=
NM_004491.4:c.8145T= NP_004482.4:n.8145T=
NM_004491.5:c.*3645T= MANE Select NP_004482.4:n.*3645T=