Canonical Allele Identifier: CA377617449

Gene: RBP4 FFAR4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93600470C>A , CM000672.2:g.93600470C>A	GRCh38
NC_000010.10:g.95360227C>A , CM000672.1:g.95360227C>A	GRCh37
NC_000010.9:g.95350217C>A	NCBI36
NG_009104.1:g.5767G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006744.4:c.278G>T (RBP4) MANE Select	NP_006735.2:p.Gly93Val
ENST00000371464.8:c.278G>T (RBP4) MANE Select	ENSP00000360519.3:p.Gly93Val
NM_001323517.1:c.278G>T (RBP4)	NP_001310446.1:p.Gly93Val
NM_001323518.1:c.272G>T (RBP4)	NP_001310447.1:p.Gly91Val
NM_001323518.2:c.272G>T (RBP4)	NP_001310447.1:p.Gly91Val
NM_006744.3:c.278G>T (RBP4)	NP_006735.2:p.Gly93Val
ENST00000371464.7:c.278G>T (RBP4)	ENSP00000360519.3:p.Gly93Val
ENST00000371467.5:c.278G>T (RBP4)	ENSP00000360522.1:p.Gly93Val
ENST00000371469.2:c.272G>T (RBP4)	ENSP00000360524.2:p.Gly91Val
ENST00000604414.1:c.697-3604C>A (FFAR4)	ENSP00000474477.1:n.697-3604C>A
ENST00000615669.4:c.272G>T (RBP4)	ENSP00000480654.1:p.Gly91Val
ENST00000629763.2:c.272G>T (RBP4)	ENSP00000487033.1:p.Gly91Val