Canonical Allele Identifier: CA1928693625

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601570_93601575delinsACCTGG , CM000672.2:g.93601570_93601575delinsACCTGG GRCh38
NC_000010.10:g.95361327_95361332delinsACCTGG , CM000672.1:g.95361327_95361332delinsACCTGG GRCh37
NC_000010.9:g.95351317_95351322delinsACCTGG NCBI36
NG_009104.1:g.4662_4667delinsCCAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371467.5:c.-232_-227delinsCCAGGT (RBP4) ENSP00000360522.1:n.-232_-227delinsCCAGGT
ENST00000371469.2:c.51+91_51+96delinsCCAGGT (RBP4) ENSP00000360524.2:n.51+91_51+96delinsCCAGGT
ENST00000604414.1:c.697-2504_697-2499delinsACCTGG (FFAR4) ENSP00000474477.1:n.697-2504_697-2499delinsACCTGG
ENST00000629763.2:c.47+95_47+100delinsCCAGGT (RBP4) ENSP00000487033.1:n.47+95_47+100delinsCCAGGT
NM_001323518.1:c.51+91_51+96delinsCCAGGT (RBP4) NP_001310447.1:n.51+91_51+96delinsCCAGGT
NM_001323518.2:c.51+91_51+96delinsCCAGGT (RBP4) NP_001310447.1:n.51+91_51+96delinsCCAGGT