Canonical Allele Identifier: CA1582747350

Gene: RAPGEF6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.131498253C= , CM000667.2:g.131498253C=	GRCh38
NC_000005.9:g.130833946C= , CM000667.1:g.130833946C=	GRCh37
NC_000005.8:g.130861845C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016340.6:c.1419+190G= MANE Select	NP_057424.3:n.1419+190G=
ENST00000509018.6:c.1419+190G= MANE Select	ENSP00000421684.1:n.1419+190G=
NM_001164386.1:c.1419+190G=	NP_001157858.1:n.1419+190G=
NM_001164386.2:c.1419+190G=	NP_001157858.1:n.1419+190G=
NM_001164387.1:c.1419+190G=	NP_001157859.1:n.1419+190G=
NM_001164387.2:c.1419+190G=	NP_001157859.1:n.1419+190G=
NM_001164388.1:c.1419+190G=	NP_001157860.1:n.1419+190G=
NM_001164388.2:c.1419+190G=	NP_001157860.1:n.1419+190G=
NM_001164389.1:c.1419+190G=	NP_001157861.1:n.1419+190G=
NM_001164389.2:c.1419+190G=	NP_001157861.1:n.1419+190G=
NM_001164390.1:c.1419+190G=	NP_001157862.1:n.1419+190G=
NM_001164390.2:c.1419+190G=	NP_001157862.1:n.1419+190G=
NM_016340.5:c.1419+190G=	NP_057424.3:n.1419+190G=
ENST00000296859.10:c.1419+190G=	ENSP00000296859.6:n.1419+190G=
ENST00000308008.10:c.1419+190G=	ENSP00000311419.6:n.1419+190G=
ENST00000507093.5:c.1419+190G=	ENSP00000426081.2:n.1419+190G=
ENST00000509018.5:c.1419+190G=	ENSP00000421684.1:n.1419+190G=
ENST00000510071.5:c.1419+190G=	ENSP00000425389.1:n.1419+190G=
ENST00000512052.5:c.564+190G=	ENSP00000426910.1:n.564+190G=
ENST00000514179.5:n.983+190G=
ENST00000514667.1:c.1569+190G=	ENSP00000426948.1:n.1569+190G=
ENST00000515170.5:c.1419+190G=	ENSP00000425772.1:n.1419+190G=
ENST00000627212.2:c.1419+190G=	ENSP00000487439.1:n.1419+190G=
ENST00000671916.1:c.417+190G=	ENSP00000500379.1:n.417+190G=