Canonical Allele Identifier: CA2339183677
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004282C= , CM000681.2:g.47004282C= GRCh38
NC_000019.9:g.47507539C= , CM000681.1:g.47507539C= GRCh37
NC_000019.8:g.52199379C= NCBI36
NG_047014.1:g.90716C=
NG_047014.2:g.148286C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8094C= ENSP00000385720.2:n.8094C=
ENST00000672722.1:c.*3594C= MANE Select ENSP00000500409.1:n.*3594C=
ENST00000404338.7:c.8094C= ENSP00000385720.2:n.8094C=
ENST00000614079.1:c.7671C= ENSP00000483730.1:n.7671C=
NM_004491.4:c.8094C= NP_004482.4:n.8094C=
NM_004491.5:c.*3594C= MANE Select NP_004482.4:n.*3594C=
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