Canonical Allele Identifier: CA2339183520
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004033A= , CM000681.2:g.47004033A= GRCh38
NC_000019.9:g.47507290A= , CM000681.1:g.47507290A= GRCh37
NC_000019.8:g.52199130A= NCBI36
NG_047014.1:g.90467A=
NG_047014.2:g.148037A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7845A= ENSP00000385720.2:n.7845A=
ENST00000672722.1:c.*3345A= MANE Select ENSP00000500409.1:n.*3345A=
ENST00000404338.7:c.7845A= ENSP00000385720.2:n.7845A=
ENST00000614079.1:c.7422A= ENSP00000483730.1:n.7422A=
NM_004491.4:c.7845A= NP_004482.4:n.7845A=
NM_004491.5:c.*3345A= MANE Select NP_004482.4:n.*3345A=
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