Canonical Allele Identifier: CA760792602

Gene: RAPGEF4

Linked Data

• dbSNP Id: rs2676527
• MyVariant Identifiers: chr2:g.173747712C>T (hg19) ; chr2:g.172882984C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.172882984C>T , CM000664.2:g.172882984C>T	GRCh38
NC_000002.11:g.173747712C>T , CM000664.1:g.173747712C>T	GRCh37
NC_000002.10:g.173455958C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000397081.8:c.445-34818C>T MANE Select	ENSP00000380271.3:n.445-34818C>T
ENST00000397081.7:c.445-34818C>T	ENSP00000380271.3:n.445-34818C>T
ENST00000397087.7:c.13-34818C>T	ENSP00000380276.3:n.13-34818C>T
ENST00000409036.5:c.445-34818C>T	ENSP00000387104.1:n.445-34818C>T
ENST00000473003.5:n.262+22685C>T
ENST00000484331.5:n.512-34818C>T
ENST00000538974.5:c.-16+22685C>T	ENSP00000440135.1:n.-16+22685C>T
ENST00000540783.5:c.-16+22685C>T	ENSP00000440250.1:n.-16+22685C>T
NM_001100397.1:c.13-34818C>T	NP_001093867.1:n.13-34818C>T
NM_001282899.1:c.-16+22685C>T	NP_001269828.1:n.-16+22685C>T
NM_001282900.1:c.-16+22685C>T	NP_001269829.1:n.-16+22685C>T
NM_007023.3:c.445-34818C>T	NP_008954.2:n.445-34818C>T
XM_005246246.1:c.445-34818C>T	XP_005246303.1:n.445-34818C>T
XM_006712205.2:c.-15-34818C>T	XP_006712268.1:n.-15-34818C>T
XM_011510505.1:c.75-34818C>T	XP_011508807.1:n.75-34818C>T
XM_005246246.3:c.445-34818C>T	XP_005246303.1:n.445-34818C>T
XM_006712205.3:c.-15-34818C>T	XP_006712268.1:n.-15-34818C>T
XM_011510505.3:c.75-34818C>T	XP_011508807.1:n.75-34818C>T
XM_017003196.2:c.445-34818C>T	XP_016858685.1:n.445-34818C>T
XM_017003197.1:c.13-34818C>T	XP_016858686.1:n.13-34818C>T
NM_007023.4:c.445-34818C>T MANE Select	NP_008954.2:n.445-34818C>T
NM_001100397.2:c.13-34818C>T	NP_001093867.1:n.13-34818C>T
NM_001282899.2:c.-16+22685C>T	NP_001269828.1:n.-16+22685C>T
NM_001282900.2:c.-16+22685C>T	NP_001269829.1:n.-16+22685C>T
NM_001375864.1:c.415-34818C>T	NP_001362793.1:n.415-34818C>T
NM_001375865.1:c.445-34818C>T	NP_001362794.1:n.445-34818C>T
NM_001375866.1:c.445-34818C>T	NP_001362795.1:n.445-34818C>T
NM_001375867.1:c.444+68559C>T	NP_001362796.1:n.444+68559C>T
NM_001375868.1:c.445-34818C>T	NP_001362797.1:n.445-34818C>T
NM_001375869.1:c.445-34818C>T	NP_001362798.1:n.445-34818C>T
NM_001375870.1:c.445-34818C>T	NP_001362799.1:n.445-34818C>T
NM_001375871.1:c.445-34818C>T	NP_001362800.1:n.445-34818C>T
NM_001375872.1:c.445-34818C>T	NP_001362801.1:n.445-34818C>T
NM_001375873.1:c.445-34818C>T	NP_001362802.1:n.445-34818C>T
NM_001375874.1:c.445-34818C>T	NP_001362803.1:n.445-34818C>T
NM_001375875.1:c.445-34818C>T	NP_001362804.1:n.445-34818C>T
NM_001375876.1:c.445-34818C>T	NP_001362805.1:n.445-34818C>T
NR_164739.1:n.584-34818C>T
NR_164740.1:n.584-34818C>T
NR_164741.1:n.584-34818C>T