Canonical Allele Identifier: CA1693940376
Gene: RAPGEF5 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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