Canonical Allele Identifier: CA2830535182

Gene: RAPGEF2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.159343378_159343379insAGGGCAGGGTCCATGTTCACT , CM000666.2:g.159343378_159343379insAGGGCAGGGTCCATGTTCACT	GRCh38
NC_000004.11:g.160264530_160264531insAGGGCAGGGTCCATGTTCACT , CM000666.1:g.160264530_160264531insAGGGCAGGGTCCATGTTCACT	GRCh37
NC_000004.10:g.160483980_160483981insAGGGCAGGGTCCATGTTCACT	NCBI36
NG_063926.1:g.244310_244311insAGGGCAGGGTCCATGTTCACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505026.2:c.2745_2746insAGGGCAGGGTCCATGTTCACT	ENSP00000516108.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
ENST00000691494.1:c.3228_3229insAGGGCAGGGTCCATGTTCACT MANE Select	ENSP00000510694.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
ENST00000644474.1:c.3210_3211insAGGGCAGGGTCCATGTTCACT	ENSP00000495906.1:p.Met1070_Asp1071insArgAlaGlySerMetPheThr
ENST00000644902.1:c.2874_2875insAGGGCAGGGTCCATGTTCACT	ENSP00000495298.1:p.Met958_Asp959insArgAlaGlySerMetPheThr
ENST00000264431.8:c.2745_2746insAGGGCAGGGTCCATGTTCACT	ENSP00000264431.4:p.Met915_Asp916insArgAlaGlySerMetPheThr
ENST00000502485.1:c.85_86insAGGGCAGGGTCCATGTTCACT
NM_014247.2:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_055062.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
XM_005263358.2:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_005263415.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_005263359.2:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_005263416.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_005263360.2:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_005263417.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_005263361.2:c.3210_3211insAGGGCAGGGTCCATGTTCACT	XP_005263418.1:p.Met1070_Asp1071insArgAlaGlySerMetPheThr
XM_006714420.2:c.3210_3211insAGGGCAGGGTCCATGTTCACT	XP_006714483.1:p.Met1070_Asp1071insArgAlaGlySerMetPheThr
XM_006714421.2:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_006714484.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_006714422.2:c.2880_2881insAGGGCAGGGTCCATGTTCACT	XP_006714485.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
XM_011532425.1:c.2892_2893insAGGGCAGGGTCCATGTTCACT	XP_011530727.1:p.Met964_Asp965insArgAlaGlySerMetPheThr
XM_011532426.1:c.2880_2881insAGGGCAGGGTCCATGTTCACT	XP_011530728.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
XM_011532427.1:c.2745_2746insAGGGCAGGGTCCATGTTCACT	XP_011530729.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_001351724.1:c.3228_3229insAGGGCAGGGTCCATGTTCACT	NP_001338653.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
NM_001351725.1:c.2880_2881insAGGGCAGGGTCCATGTTCACT	NP_001338654.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
NM_001351726.1:c.2880_2881insAGGGCAGGGTCCATGTTCACT	NP_001338655.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
NM_001351727.1:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_001338656.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_001351728.1:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_001338657.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
XM_005263358.3:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_005263415.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_005263359.4:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_005263416.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_005263360.3:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_005263417.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_005263361.3:c.3210_3211insAGGGCAGGGTCCATGTTCACT	XP_005263418.1:p.Met1070_Asp1071insArgAlaGlySerMetPheThr
XM_006714420.3:c.3210_3211insAGGGCAGGGTCCATGTTCACT	XP_006714483.1:p.Met1070_Asp1071insArgAlaGlySerMetPheThr
XM_006714422.4:c.2880_2881insAGGGCAGGGTCCATGTTCACT	XP_006714485.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
XM_011532425.2:c.2892_2893insAGGGCAGGGTCCATGTTCACT	XP_011530727.1:p.Met964_Asp965insArgAlaGlySerMetPheThr
XM_011532426.2:c.2880_2881insAGGGCAGGGTCCATGTTCACT	XP_011530728.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
XM_017008856.2:c.3228_3229insAGGGCAGGGTCCATGTTCACT	XP_016864345.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
XM_024454286.1:c.2862_2863insAGGGCAGGGTCCATGTTCACT	XP_024310054.1:p.Met954_Asp955insArgAlaGlySerMetPheThr
XM_024454287.1:c.2862_2863insAGGGCAGGGTCCATGTTCACT	XP_024310055.1:p.Met954_Asp955insArgAlaGlySerMetPheThr
NM_001351724.2:c.3228_3229insAGGGCAGGGTCCATGTTCACT	NP_001338653.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
NM_001351727.2:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_001338656.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_001351728.2:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_001338657.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_014247.3:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_055062.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_001351724.4:c.3228_3229insAGGGCAGGGTCCATGTTCACT	NP_001338653.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
NM_001351725.2:c.2880_2881insAGGGCAGGGTCCATGTTCACT	NP_001338654.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
NM_001351726.3:c.2880_2881insAGGGCAGGGTCCATGTTCACT	NP_001338655.1:p.Met960_Asp961insArgAlaGlySerMetPheThr
NM_001351727.4:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_001338656.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_001351728.4:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_001338657.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_001394067.1:c.3228_3229insAGGGCAGGGTCCATGTTCACT	NP_001380996.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
NM_014247.5:c.2745_2746insAGGGCAGGGTCCATGTTCACT	NP_055062.1:p.Met915_Asp916insArgAlaGlySerMetPheThr
NM_001351724.5:c.3228_3229insAGGGCAGGGTCCATGTTCACT	NP_001338653.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr
NM_001394067.2:c.3228_3229insAGGGCAGGGTCCATGTTCACT MANE Select	NP_001380996.1:p.Met1076_Asp1077insArgAlaGlySerMetPheThr