Canonical Allele Identifier: CA211552438

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs981452705
• MyVariant Identifiers: chr10:g.95356967A>T (hg19) ; chr10:g.93597210A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93597210A>T , CM000672.2:g.93597210A>T	GRCh38
NC_000010.10:g.95356967A>T , CM000672.1:g.95356967A>T	GRCh37
NC_000010.9:g.95346957A>T	NCBI36
NG_009104.1:g.9027T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371464.8:c.356-3175T>A (RBP4) MANE Select	ENSP00000360519.3:n.356-3175T>A
ENST00000371464.7:c.356-3175T>A (RBP4)	ENSP00000360519.3:n.356-3175T>A
ENST00000371467.5:c.356-3175T>A (RBP4)	ENSP00000360522.1:n.356-3175T>A
ENST00000371469.2:c.350-3175T>A (RBP4)	ENSP00000360524.2:n.350-3175T>A
ENST00000604414.1:c.697-6864A>T (FFAR4)	ENSP00000474477.1:n.697-6864A>T
ENST00000615669.4:c.350-3175T>A (RBP4)	ENSP00000480654.1:n.350-3175T>A
ENST00000629763.2:c.350-3175T>A (RBP4)	ENSP00000487033.1:n.350-3175T>A
NM_006744.3:c.356-3175T>A (RBP4)	NP_006735.2:n.356-3175T>A
NM_001323517.1:c.356-3175T>A (RBP4)	NP_001310446.1:n.356-3175T>A
NM_001323518.1:c.350-3175T>A (RBP4)	NP_001310447.1:n.350-3175T>A
NM_006744.4:c.356-3175T>A (RBP4) MANE Select	NP_006735.2:n.356-3175T>A
NM_001323518.2:c.350-3175T>A (RBP4)	NP_001310447.1:n.350-3175T>A