Canonical Allele Identifier: CA2339183400
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003845G= , CM000681.2:g.47003845G= GRCh38
NC_000019.9:g.47507102G= , CM000681.1:g.47507102G= GRCh37
NC_000019.8:g.52198942G= NCBI36
NG_047014.1:g.90279G=
NG_047014.2:g.147849G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7657G= ENSP00000385720.2:n.7657G=
ENST00000672722.1:c.*3157G= MANE Select ENSP00000500409.1:n.*3157G=
ENST00000404338.7:c.7657G= ENSP00000385720.2:n.7657G=
ENST00000614079.1:c.7234G= ENSP00000483730.1:n.7234G=
NM_004491.4:c.7657G= NP_004482.4:n.7657G=
NM_004491.5:c.*3157G= MANE Select NP_004482.4:n.*3157G=
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