Canonical Allele Identifier: CA2339183411
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003873T= , CM000681.2:g.47003873T= GRCh38
NC_000019.9:g.47507130T= , CM000681.1:g.47507130T= GRCh37
NC_000019.8:g.52198970T= NCBI36
NG_047014.1:g.90307T=
NG_047014.2:g.147877T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7685T= ENSP00000385720.2:n.7685T=
ENST00000672722.1:c.*3185T= MANE Select ENSP00000500409.1:n.*3185T=
ENST00000404338.7:c.7685T= ENSP00000385720.2:n.7685T=
ENST00000614079.1:c.7262T= ENSP00000483730.1:n.7262T=
NM_004491.4:c.7685T= NP_004482.4:n.7685T=
NM_004491.5:c.*3185T= MANE Select NP_004482.4:n.*3185T=
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