Canonical Allele Identifier: CA377617051

Gene: RBP4 FFAR4

Linked Data

• ClinVar Variation Id: 493081
• ClinVar RCV Id: RCV000585464
• dbSNP Id: rs1554887443
• COSMIC: COSM3441679 ; COSM3441680
• MyVariant Identifiers: chr10:g.95360152C>T (hg19) ; chr10:g.93600395C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93600395C>T , CM000672.2:g.93600395C>T	GRCh38
NC_000010.10:g.95360152C>T , CM000672.1:g.95360152C>T	GRCh37
NC_000010.9:g.95350142C>T	NCBI36
NG_009104.1:g.5842G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371464.8:c.353G>A (RBP4) MANE Select	ENSP00000360519.3:p.Gly118Glu
ENST00000371464.7:c.353G>A (RBP4)	ENSP00000360519.3:p.Gly118Glu
ENST00000371467.5:c.353G>A (RBP4)	ENSP00000360522.1:p.Gly118Glu
ENST00000371469.2:c.347G>A (RBP4)	ENSP00000360524.2:p.Gly116Glu
ENST00000604414.1:c.697-3679C>T (FFAR4)	ENSP00000474477.1:n.697-3679C>T
ENST00000615669.4:c.347G>A (RBP4)	ENSP00000480654.1:p.Gly116Glu
ENST00000629763.2:c.347G>A (RBP4)	ENSP00000487033.1:p.Gly116Glu
NM_006744.3:c.353G>A (RBP4)	NP_006735.2:p.Gly118Glu
NM_001323517.1:c.353G>A (RBP4)	NP_001310446.1:p.Gly118Glu
NM_001323518.1:c.347G>A (RBP4)	NP_001310447.1:p.Gly116Glu
NM_006744.4:c.353G>A (RBP4) MANE Select	NP_006735.2:p.Gly118Glu
NM_001323518.2:c.347G>A (RBP4)	NP_001310447.1:p.Gly116Glu