Canonical Allele Identifier: CA2339183719
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004335C= , CM000681.2:g.47004335C= GRCh38
NC_000019.9:g.47507592C= , CM000681.1:g.47507592C= GRCh37
NC_000019.8:g.52199432C= NCBI36
NG_047014.1:g.90769C=
NG_047014.2:g.148339C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8147C= ENSP00000385720.2:n.8147C=
ENST00000672722.1:c.*3647C= MANE Select ENSP00000500409.1:n.*3647C=
ENST00000404338.7:c.8147C= ENSP00000385720.2:n.8147C=
NM_004491.4:c.8147C= NP_004482.4:n.8147C=
NM_004491.5:c.*3647C= MANE Select NP_004482.4:n.*3647C=