Canonical Allele Identifier: CA1693940373

Gene: RAPGEF5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22329059T= , CM000669.2:g.22329059T=	GRCh38
NC_000007.13:g.22368678T= , CM000669.1:g.22368678T=	GRCh37
NC_000007.12:g.22335203T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012294.5:c.232-11022A= MANE Select	NP_036426.4:n.232-11022A=
ENST00000665637.1:c.232-11022A= MANE Select	ENSP00000499535.1:n.232-11022A=
NM_012294.3:c.-228-11022A=	NP_036426.3:n.-228-11022A=
NM_012294.4:c.232-11022A=	NP_036426.4:n.232-11022A=
ENST00000344041.10:c.-228-11022A=	ENSP00000343656.6:n.-228-11022A=
ENST00000405243.1:c.232-11022A=	ENSP00000384870.1:n.232-11022A=
ENST00000471484.1:n.249-11022A=
XM_005249914.2:c.232-11022A=	XP_005249971.1:n.232-11022A=
XM_005249916.1:c.-228-11022A=	XP_005249973.1:n.-228-11022A=