Canonical Allele Identifier: CA2722330604

Linked Data

dbSNP Id: rs36035572

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93593487dup , CM000672.2:g.93593487dup GRCh38
NC_000010.10:g.95353244dup , CM000672.1:g.95353244dup GRCh37
NC_000010.9:g.95343234dup NCBI36
NG_009104.1:g.12751dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371464.8:c.568+337dup (RBP4) MANE Select ENSP00000360519.3:n.568+337dup
ENST00000371464.7:c.568+337dup (RBP4) ENSP00000360519.3:n.568+337dup
ENST00000371467.5:c.568+337dup (RBP4) ENSP00000360522.1:n.568+337dup
ENST00000371469.2:c.562+337dup (RBP4) ENSP00000360524.2:n.562+337dup
ENST00000604414.1:c.697-10587dup (FFAR4) ENSP00000474477.1:n.697-10587dup
ENST00000615669.4:c.562+337dup (RBP4) ENSP00000480654.1:n.562+337dup
ENST00000629763.2:c.562+337dup (RBP4) ENSP00000487033.1:n.562+337dup
NM_006744.3:c.568+337dup (RBP4) NP_006735.2:n.568+337dup
NM_001323517.1:c.568+337dup (RBP4) NP_001310446.1:n.568+337dup
NM_001323518.1:c.562+337dup (RBP4) NP_001310447.1:n.562+337dup
NM_006744.4:c.568+337dup (RBP4) MANE Select NP_006735.2:n.568+337dup
NM_001323518.2:c.562+337dup (RBP4) NP_001310447.1:n.562+337dup