Canonical Allele Identifier: CA108901856
Gene: RAPGEF2 HGNC NCBI

Linked Data

dbSNP Id: rs555035867

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.159341691A>C , CM000666.2:g.159341691A>C GRCh38
NC_000004.11:g.160262843A>C , CM000666.1:g.160262843A>C GRCh37
NC_000004.10:g.160482293A>C NCBI36
NG_063926.1:g.242623A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000505026.2:c.2179A>C ENSP00000516108.1:p.Met727Leu
ENST00000691494.1:c.2662A>C MANE Select ENSP00000510694.1:p.Met888Leu
ENST00000644474.1:c.2644A>C ENSP00000495906.1:p.Met882Leu
ENST00000644902.1:c.2308A>C ENSP00000495298.1:p.Met770Leu
ENST00000264431.8:c.2179A>C ENSP00000264431.4:p.Met727Leu
NM_014247.2:c.2179A>C NP_055062.1:p.Met727Leu
XM_005263358.2:c.2662A>C XP_005263415.1:p.Met888Leu
XM_005263359.2:c.2662A>C XP_005263416.1:p.Met888Leu
XM_005263360.2:c.2662A>C XP_005263417.1:p.Met888Leu
XM_005263361.2:c.2644A>C XP_005263418.1:p.Met882Leu
XM_006714420.2:c.2644A>C XP_006714483.1:p.Met882Leu
XM_006714421.2:c.2662A>C XP_006714484.1:p.Met888Leu
XM_006714422.2:c.2314A>C XP_006714485.1:p.Met772Leu
XM_011532425.1:c.2326A>C XP_011530727.1:p.Met776Leu
XM_011532426.1:c.2314A>C XP_011530728.1:p.Met772Leu
XM_011532427.1:c.2179A>C XP_011530729.1:p.Met727Leu
NM_001351724.1:c.2662A>C NP_001338653.1:p.Met888Leu
NM_001351725.1:c.2314A>C NP_001338654.1:p.Met772Leu
NM_001351726.1:c.2314A>C NP_001338655.1:p.Met772Leu
NM_001351727.1:c.2179A>C NP_001338656.1:p.Met727Leu
NM_001351728.1:c.2179A>C NP_001338657.1:p.Met727Leu
XM_005263358.3:c.2662A>C XP_005263415.1:p.Met888Leu
XM_005263359.4:c.2662A>C XP_005263416.1:p.Met888Leu
XM_005263360.3:c.2662A>C XP_005263417.1:p.Met888Leu
XM_005263361.3:c.2644A>C XP_005263418.1:p.Met882Leu
XM_006714420.3:c.2644A>C XP_006714483.1:p.Met882Leu
XM_006714422.4:c.2314A>C XP_006714485.1:p.Met772Leu
XM_011532425.2:c.2326A>C XP_011530727.1:p.Met776Leu
XM_011532426.2:c.2314A>C XP_011530728.1:p.Met772Leu
XM_017008856.2:c.2662A>C XP_016864345.1:p.Met888Leu
XM_024454286.1:c.2296A>C XP_024310054.1:p.Met766Leu
XM_024454287.1:c.2296A>C XP_024310055.1:p.Met766Leu
NM_001351724.2:c.2662A>C NP_001338653.1:p.Met888Leu
NM_001351727.2:c.2179A>C NP_001338656.1:p.Met727Leu
NM_001351728.2:c.2179A>C NP_001338657.1:p.Met727Leu
NM_014247.3:c.2179A>C NP_055062.1:p.Met727Leu
NM_001351724.4:c.2662A>C NP_001338653.1:p.Met888Leu
NM_001351725.2:c.2314A>C NP_001338654.1:p.Met772Leu
NM_001351726.3:c.2314A>C NP_001338655.1:p.Met772Leu
NM_001351727.4:c.2179A>C NP_001338656.1:p.Met727Leu
NM_001351728.4:c.2179A>C NP_001338657.1:p.Met727Leu
NM_001394067.1:c.2662A>C NP_001380996.1:p.Met888Leu
NM_014247.5:c.2179A>C NP_055062.1:p.Met727Leu
NM_001351724.5:c.2662A>C NP_001338653.1:p.Met888Leu
NM_001394067.2:c.2662A>C MANE Select NP_001380996.1:p.Met888Leu