Canonical Allele Identifier: CA238406173
Gene: RAP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68656982dup , CM000674.2:g.68656982dup GRCh38
NC_000012.11:g.69050762dup , CM000674.1:g.69050762dup GRCh37
NC_000012.10:g.67337029dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250559.14:c.469-119dup MANE Select ENSP00000250559.9:n.469-119dup
ENST00000250559.13:c.469-119dup ENSP00000250559.9:n.469-119dup
ENST00000341355.9:c.469-119dup ENSP00000441275.1:n.469-119dup
ENST00000378985.7:c.271-119dup ENSP00000368270.3:n.271-119dup
ENST00000393436.9:c.469-119dup ENSP00000377085.5:n.469-119dup
ENST00000425247.6:c.468+533dup ENSP00000401095.2:n.468+533dup
ENST00000450214.6:c.343-119dup ENSP00000399986.2:n.343-119dup
ENST00000463493.5:n.447-119dup
ENST00000535492.5:c.271-119dup ENSP00000443775.1:n.271-119dup
ENST00000537460.5:c.469-119dup ENSP00000439966.1:n.469-119dup
ENST00000538980.5:c.316-119dup ENSP00000444467.1:n.316-119dup
ENST00000539091.5:c.343-119dup ENSP00000444830.1:n.343-119dup
ENST00000540209.5:c.412-119dup ENSP00000446318.1:n.412-119dup
ENST00000542145.5:c.328-119dup ENSP00000440014.1:n.328-119dup
ENST00000543393.5:c.271-119dup ENSP00000445090.1:n.271-119dup
ENST00000543697.5:c.325-119dup ENSP00000440708.1:n.325-119dup
NM_001010942.2:c.469-119dup NP_001010942.1:n.469-119dup
NM_001251917.1:c.343-119dup NP_001238846.1:n.343-119dup
NM_001251918.1:c.343-119dup NP_001238847.1:n.343-119dup
NM_001251921.1:c.412-119dup NP_001238850.1:n.412-119dup
NM_001251922.1:c.328-119dup NP_001238851.1:n.328-119dup
NM_015646.5:c.469-119dup NP_056461.1:n.469-119dup
NM_001010942.3:c.469-119dup MANE Select NP_001010942.1:n.469-119dup
NM_001251917.2:c.343-119dup NP_001238846.1:n.343-119dup
NM_001251918.2:c.343-119dup NP_001238847.1:n.343-119dup
NM_001251921.2:c.412-119dup NP_001238850.1:n.412-119dup
NM_001251922.2:c.328-119dup NP_001238851.1:n.328-119dup
NM_015646.6:c.469-119dup NP_056461.1:n.469-119dup