Canonical Allele Identifier: CA1928693688
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs2058340330
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601639_93601650del , CM000672.2:g.93601639_93601650del GRCh38
NC_000010.10:g.95361396_95361407del , CM000672.1:g.95361396_95361407del GRCh37
NC_000010.9:g.95351386_95351397del NCBI36
NG_009104.1:g.4590_4601del

Transcript Alleles

HGVS Amino-acid change
ENST00000371467.5:c.-304_-293del (RBP4) ENSP00000360522.1:n.-304_-293del
ENST00000371469.2:c.51+19_51+30del (RBP4) ENSP00000360524.2:n.51+19_51+30del
ENST00000604414.1:c.697-2435_697-2424del (FFAR4) ENSP00000474477.1:n.697-2435_697-2424del
ENST00000629763.2:c.47+23_47+34del (RBP4) ENSP00000487033.1:n.47+23_47+34del
NM_001323518.1:c.51+19_51+30del (RBP4) NP_001310447.1:n.51+19_51+30del
NM_001323518.2:c.51+19_51+30del (RBP4) NP_001310447.1:n.51+19_51+30del
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