Canonical Allele Identifier: CA6677172

Gene: RAP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68656386A>G , CM000674.2:g.68656386A>G	GRCh38
NC_000012.11:g.69050166A>G , CM000674.1:g.69050166A>G	GRCh37
NC_000012.10:g.67336433A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250559.14:c.405A>G MANE Select	ENSP00000250559.9:p.Ala135=
ENST00000250559.13:c.405A>G	ENSP00000250559.9:p.Ala135=
ENST00000341355.9:c.405A>G	ENSP00000441275.1:p.Ala135=
ENST00000378985.7:c.207A>G	ENSP00000368270.3:p.Ala69=
ENST00000393436.9:c.405A>G	ENSP00000377085.5:p.Ala135=
ENST00000425247.6:c.405A>G	ENSP00000401095.2:p.Ala135=
ENST00000450214.6:c.279A>G	ENSP00000399986.2:p.Ala93=
ENST00000463493.5:n.383A>G
ENST00000535492.5:c.207A>G	ENSP00000443775.1:p.Ala69=
ENST00000537460.5:c.405A>G	ENSP00000439966.1:p.Ala135=
ENST00000538980.5:c.252A>G	ENSP00000444467.1:p.Ala84=
ENST00000539091.5:c.279A>G	ENSP00000444830.1:p.Ala93=
ENST00000540209.5:c.348A>G	ENSP00000446318.1:p.Ala116=
ENST00000540781.5:c.405A>G	ENSP00000440466.1:p.Ala135=
ENST00000541216.1:c.405A>G	ENSP00000443851.1:p.Ala135=
ENST00000542145.5:c.264A>G	ENSP00000440014.1:p.Ala88=
ENST00000543393.5:c.207A>G	ENSP00000445090.1:p.Ala69=
ENST00000543697.5:c.325-715A>G	ENSP00000440708.1:n.325-715A>G
ENST00000544639.1:n.504A>G
NM_001010942.2:c.405A>G	NP_001010942.1:p.Ala135=
NM_001251917.1:c.279A>G	NP_001238846.1:p.Ala93=
NM_001251918.1:c.279A>G	NP_001238847.1:p.Ala93=
NM_001251921.1:c.348A>G	NP_001238850.1:p.Ala116=
NM_001251922.1:c.264A>G	NP_001238851.1:p.Ala88=
NM_015646.5:c.405A>G	NP_056461.1:p.Ala135=
NM_001010942.3:c.405A>G MANE Select	NP_001010942.1:p.Ala135=
NM_001251917.2:c.279A>G	NP_001238846.1:p.Ala93=
NM_001251918.2:c.279A>G	NP_001238847.1:p.Ala93=
NM_001251921.2:c.348A>G	NP_001238850.1:p.Ala116=
NM_001251922.2:c.264A>G	NP_001238851.1:p.Ala88=
NM_015646.6:c.405A>G	NP_056461.1:p.Ala135=