Canonical Allele Identifier: CA2339183679
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004283G= , CM000681.2:g.47004283G= GRCh38
NC_000019.9:g.47507540G= , CM000681.1:g.47507540G= GRCh37
NC_000019.8:g.52199380G= NCBI36
NG_047014.1:g.90717G=
NG_047014.2:g.148287G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8095G= ENSP00000385720.2:n.8095G=
ENST00000672722.1:c.*3595G= MANE Select ENSP00000500409.1:n.*3595G=
ENST00000404338.7:c.8095G= ENSP00000385720.2:n.8095G=
ENST00000614079.1:c.7672G= ENSP00000483730.1:n.7672G=
NM_004491.4:c.8095G= NP_004482.4:n.8095G=
NM_004491.5:c.*3595G= MANE Select NP_004482.4:n.*3595G=
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