Canonical Allele Identifier: CA2672534809
Gene: RAPGEF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.159341471C>A , CM000666.2:g.159341471C>A GRCh38
NC_000004.11:g.160262623C>A , CM000666.1:g.160262623C>A GRCh37
NC_000004.10:g.160482073C>A NCBI36
NG_063926.1:g.242403C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000505026.2:c.2052-93C>A ENSP00000516108.1:n.2052-93C>A
ENST00000691494.1:c.2535-93C>A MANE Select ENSP00000510694.1:n.2535-93C>A
ENST00000644474.1:c.2517-93C>A ENSP00000495906.1:n.2517-93C>A
ENST00000644902.1:c.2181-93C>A ENSP00000495298.1:n.2181-93C>A
ENST00000264431.8:c.2052-93C>A ENSP00000264431.4:n.2052-93C>A
NM_014247.2:c.2052-93C>A NP_055062.1:n.2052-93C>A
XM_005263358.2:c.2535-93C>A XP_005263415.1:n.2535-93C>A
XM_005263359.2:c.2535-93C>A XP_005263416.1:n.2535-93C>A
XM_005263360.2:c.2535-93C>A XP_005263417.1:n.2535-93C>A
XM_005263361.2:c.2517-93C>A XP_005263418.1:n.2517-93C>A
XM_006714420.2:c.2517-93C>A XP_006714483.1:n.2517-93C>A
XM_006714421.2:c.2535-93C>A XP_006714484.1:n.2535-93C>A
XM_006714422.2:c.2187-93C>A XP_006714485.1:n.2187-93C>A
XM_011532425.1:c.2199-93C>A XP_011530727.1:n.2199-93C>A
XM_011532426.1:c.2187-93C>A XP_011530728.1:n.2187-93C>A
XM_011532427.1:c.2052-93C>A XP_011530729.1:n.2052-93C>A
NM_001351724.1:c.2535-93C>A NP_001338653.1:n.2535-93C>A
NM_001351725.1:c.2187-93C>A NP_001338654.1:n.2187-93C>A
NM_001351726.1:c.2187-93C>A NP_001338655.1:n.2187-93C>A
NM_001351727.1:c.2052-93C>A NP_001338656.1:n.2052-93C>A
NM_001351728.1:c.2052-93C>A NP_001338657.1:n.2052-93C>A
XM_005263358.3:c.2535-93C>A XP_005263415.1:n.2535-93C>A
XM_005263359.4:c.2535-93C>A XP_005263416.1:n.2535-93C>A
XM_005263360.3:c.2535-93C>A XP_005263417.1:n.2535-93C>A
XM_005263361.3:c.2517-93C>A XP_005263418.1:n.2517-93C>A
XM_006714420.3:c.2517-93C>A XP_006714483.1:n.2517-93C>A
XM_006714422.4:c.2187-93C>A XP_006714485.1:n.2187-93C>A
XM_011532425.2:c.2199-93C>A XP_011530727.1:n.2199-93C>A
XM_011532426.2:c.2187-93C>A XP_011530728.1:n.2187-93C>A
XM_017008856.2:c.2535-93C>A XP_016864345.1:n.2535-93C>A
XM_024454286.1:c.2169-93C>A XP_024310054.1:n.2169-93C>A
XM_024454287.1:c.2169-93C>A XP_024310055.1:n.2169-93C>A
NM_001351724.2:c.2535-93C>A NP_001338653.1:n.2535-93C>A
NM_001351727.2:c.2052-93C>A NP_001338656.1:n.2052-93C>A
NM_001351728.2:c.2052-93C>A NP_001338657.1:n.2052-93C>A
NM_014247.3:c.2052-93C>A NP_055062.1:n.2052-93C>A
NM_001351724.4:c.2535-93C>A NP_001338653.1:n.2535-93C>A
NM_001351725.2:c.2187-93C>A NP_001338654.1:n.2187-93C>A
NM_001351726.3:c.2187-93C>A NP_001338655.1:n.2187-93C>A
NM_001351727.4:c.2052-93C>A NP_001338656.1:n.2052-93C>A
NM_001351728.4:c.2052-93C>A NP_001338657.1:n.2052-93C>A
NM_001394067.1:c.2535-93C>A NP_001380996.1:n.2535-93C>A
NM_014247.5:c.2052-93C>A NP_055062.1:n.2052-93C>A
NM_001351724.5:c.2535-93C>A NP_001338653.1:n.2535-93C>A
NM_001394067.2:c.2535-93C>A MANE Select NP_001380996.1:n.2535-93C>A