Canonical Allele Identifier: CA2339183474
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003947C= , CM000681.2:g.47003947C= GRCh38
NC_000019.9:g.47507204C= , CM000681.1:g.47507204C= GRCh37
NC_000019.8:g.52199044C= NCBI36
NG_047014.1:g.90381C=
NG_047014.2:g.147951C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7759C= ENSP00000385720.2:n.7759C=
ENST00000672722.1:c.*3259C= MANE Select ENSP00000500409.1:n.*3259C=
ENST00000404338.7:c.7759C= ENSP00000385720.2:n.7759C=
ENST00000614079.1:c.7336C= ENSP00000483730.1:n.7336C=
NM_004491.4:c.7759C= NP_004482.4:n.7759C=
NM_004491.5:c.*3259C= MANE Select NP_004482.4:n.*3259C=
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