Canonical Allele Identifier: CA1928694529

Gene: RBP4 FFAR4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93597254T= , CM000672.2:g.93597254T=	GRCh38
NC_000010.10:g.95357011T= , CM000672.1:g.95357011T=	GRCh37
NC_000010.9:g.95347001T=	NCBI36
NG_009104.1:g.8983A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371464.8:c.355+3139A= (RBP4) MANE Select	ENSP00000360519.3:n.355+3139A=
ENST00000371464.7:c.355+3139A= (RBP4)	ENSP00000360519.3:n.355+3139A=
ENST00000371467.5:c.355+3139A= (RBP4)	ENSP00000360522.1:n.355+3139A=
ENST00000371469.2:c.349+3139A= (RBP4)	ENSP00000360524.2:n.349+3139A=
ENST00000604414.1:c.697-6820T= (FFAR4)	ENSP00000474477.1:n.697-6820T=
ENST00000615669.4:c.349+3139A= (RBP4)	ENSP00000480654.1:n.349+3139A=
ENST00000629763.2:c.349+3139A= (RBP4)	ENSP00000487033.1:n.349+3139A=
NM_006744.3:c.355+3139A= (RBP4)	NP_006735.2:n.355+3139A=
NM_001323517.1:c.355+3139A= (RBP4)	NP_001310446.1:n.355+3139A=
NM_001323518.1:c.349+3139A= (RBP4)	NP_001310447.1:n.349+3139A=
NM_006744.4:c.355+3139A= (RBP4) MANE Select	NP_006735.2:n.355+3139A=
NM_001323518.2:c.349+3139A= (RBP4)	NP_001310447.1:n.349+3139A=