Canonical Allele Identifier: CA1928693717

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601673_93601674delinsTG , CM000672.2:g.93601673_93601674delinsTG GRCh38
NC_000010.10:g.95361430_95361431delinsTG , CM000672.1:g.95361430_95361431delinsTG GRCh37
NC_000010.9:g.95351420_95351421delinsTG NCBI36
NG_009104.1:g.4563_4564delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.43_44delinsCA (RBP4) ENSP00000360524.2:p.Gln15=
ENST00000604414.1:c.697-2401_697-2400delinsTG (FFAR4) ENSP00000474477.1:n.697-2401_697-2400delinsTG
ENST00000629763.2:c.43_44delinsCA (RBP4) ENSP00000487033.1:p.Gln15=
NM_001323518.1:c.43_44delinsCA (RBP4) NP_001310447.1:p.Gln15=
NM_001323518.2:c.43_44delinsCA (RBP4) NP_001310447.1:p.Gln15=