Canonical Allele Identifier: CA1307950219
Gene: RAPGEF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.172755737G>C , CM000664.2:g.172755737G>C GRCh38
NC_000002.11:g.173620465G>C , CM000664.1:g.173620465G>C GRCh37
NC_000002.10:g.173328711G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397081.8:c.65+19689G>C MANE Select ENSP00000380271.3:n.65+19689G>C
ENST00000397081.7:c.65+19689G>C ENSP00000380271.3:n.65+19689G>C
ENST00000409036.5:c.65+19689G>C ENSP00000387104.1:n.65+19689G>C
ENST00000464976.1:n.286+11314G>C
ENST00000484331.5:n.132+20332G>C
NM_007023.3:c.65+19689G>C NP_008954.2:n.65+19689G>C
XM_005246246.1:c.65+19689G>C XP_005246303.1:n.65+19689G>C
XM_006712205.2:c.-395+20332G>C XP_006712268.1:n.-395+20332G>C
XM_011510505.1:c.-306+19689G>C XP_011508807.1:n.-306+19689G>C
XM_005246246.3:c.65+19689G>C XP_005246303.1:n.65+19689G>C
XM_006712205.3:c.-395+20332G>C XP_006712268.1:n.-395+20332G>C
XM_011510505.3:c.-306+19689G>C XP_011508807.1:n.-306+19689G>C
XM_017003196.2:c.65+19689G>C XP_016858685.1:n.65+19689G>C
NM_007023.4:c.65+19689G>C MANE Select NP_008954.2:n.65+19689G>C
NM_001375864.1:c.35+19312G>C NP_001362793.1:n.35+19312G>C
NM_001375865.1:c.65+19689G>C NP_001362794.1:n.65+19689G>C
NM_001375866.1:c.65+19689G>C NP_001362795.1:n.65+19689G>C
NM_001375867.1:c.65+19689G>C NP_001362796.1:n.65+19689G>C
NM_001375868.1:c.65+19689G>C NP_001362797.1:n.65+19689G>C
NM_001375869.1:c.65+19689G>C NP_001362798.1:n.65+19689G>C
NM_001375870.1:c.65+19689G>C NP_001362799.1:n.65+19689G>C
NM_001375871.1:c.65+19689G>C NP_001362800.1:n.65+19689G>C
NM_001375872.1:c.65+19689G>C NP_001362801.1:n.65+19689G>C
NM_001375873.1:c.65+19689G>C NP_001362802.1:n.65+19689G>C
NM_001375874.1:c.65+19689G>C NP_001362803.1:n.65+19689G>C
NM_001375875.1:c.65+19689G>C NP_001362804.1:n.65+19689G>C
NM_001375876.1:c.65+19689G>C NP_001362805.1:n.65+19689G>C
NR_164739.1:n.204+19689G>C
NR_164740.1:n.204+19689G>C
NR_164741.1:n.204+19689G>C