Canonical Allele Identifier: CA1928693647

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601598_93601600delinsAGC , CM000672.2:g.93601598_93601600delinsAGC GRCh38
NC_000010.10:g.95361355_95361357delinsAGC , CM000672.1:g.95361355_95361357delinsAGC GRCh37
NC_000010.9:g.95351345_95351347delinsAGC NCBI36
NG_009104.1:g.4637_4639delinsGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371467.5:c.-257_-255delinsGCT (RBP4) ENSP00000360522.1:n.-257_-255delinsGCT
ENST00000371469.2:c.51+66_51+68delinsGCT (RBP4) ENSP00000360524.2:n.51+66_51+68delinsGCT
ENST00000604414.1:c.697-2476_697-2474delinsAGC (FFAR4) ENSP00000474477.1:n.697-2476_697-2474delinsAGC
ENST00000629763.2:c.47+70_47+72delinsGCT (RBP4) ENSP00000487033.1:n.47+70_47+72delinsGCT
NM_001323518.1:c.51+66_51+68delinsGCT (RBP4) NP_001310447.1:n.51+66_51+68delinsGCT
NM_001323518.2:c.51+66_51+68delinsGCT (RBP4) NP_001310447.1:n.51+66_51+68delinsGCT