Canonical Allele Identifier: CA11260289
Gene: RAPGEF4 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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