Canonical Allele Identifier: CA1928693724

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601675C= , CM000672.2:g.93601675C= GRCh38
NC_000010.10:g.95361432C= , CM000672.1:g.95361432C= GRCh37
NC_000010.9:g.95351422C= NCBI36
NG_009104.1:g.4562G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.42G= (RBP4) ENSP00000360524.2:p.Arg14=
ENST00000604414.1:c.697-2399C= (FFAR4) ENSP00000474477.1:n.697-2399C=
ENST00000629763.2:c.42G= (RBP4) ENSP00000487033.1:p.Arg14=
NM_001323518.1:c.42G= (RBP4) NP_001310447.1:p.Arg14=
NM_001323518.2:c.42G= (RBP4) NP_001310447.1:p.Arg14=