Canonical Allele Identifier: CA122832
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 13067
ClinVar RCV Id: RCV000013942 RCV001222967
dbSNP Id: rs121918584
gnomAD v4: 10-93600739-A-T
MyVariant Identifiers: chr10:g.95360496A>T (hg19) chr10:g.93600739A>T (hg38)
PubMed: PMID:9888420 PMID:16157297
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93600739A>T , CM000672.2:g.93600739A>T GRCh38
NC_000010.10:g.95360496A>T , CM000672.1:g.95360496A>T GRCh37
NC_000010.9:g.95350486A>T NCBI36
NG_009104.1:g.5498T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371464.8:c.176T>A (RBP4) MANE Select ENSP00000360519.3:p.Ile59Asn
ENST00000371464.7:c.176T>A (RBP4) ENSP00000360519.3:p.Ile59Asn
ENST00000371467.5:c.176T>A (RBP4) ENSP00000360522.1:p.Ile59Asn
ENST00000371469.2:c.170T>A (RBP4) ENSP00000360524.2:p.Ile57Asn
ENST00000604414.1:c.697-3335A>T (FFAR4) ENSP00000474477.1:n.697-3335A>T
ENST00000615669.4:c.170T>A (RBP4) ENSP00000480654.1:p.Ile57Asn
ENST00000629763.2:c.170T>A (RBP4) ENSP00000487033.1:p.Ile57Asn
NM_006744.3:c.176T>A (RBP4) NP_006735.2:p.Ile59Asn
NM_001323517.1:c.176T>A (RBP4) NP_001310446.1:p.Ile59Asn
NM_001323518.1:c.170T>A (RBP4) NP_001310447.1:p.Ile57Asn
NM_006744.4:c.176T>A (RBP4) MANE Select NP_006735.2:p.Ile59Asn
NM_001323518.2:c.170T>A (RBP4) NP_001310447.1:p.Ile57Asn
Search 100 bp 5'
Search 100 bp 3'