Canonical Allele Identifier: CA1928693776

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601707_93601714delinsAATAATTC , CM000672.2:g.93601707_93601714delinsAATAATTC GRCh38
NC_000010.10:g.95361464_95361471delinsAATAATTC , CM000672.1:g.95361464_95361471delinsAATAATTC GRCh37
NC_000010.9:g.95351454_95351461delinsAATAATTC NCBI36
NG_009104.1:g.4523_4530delinsGAATTATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.3_10delinsGAATTATT (RBP4) ENSP00000360524.2:p.Met1=
ENST00000604414.1:c.697-2367_697-2360delinsAATAATTC (FFAR4) ENSP00000474477.1:n.697-2367_697-2360delinsAATAATTC
ENST00000629763.2:c.3_10delinsGAATTATT (RBP4) ENSP00000487033.1:p.Met1=
NM_001323518.1:c.3_10delinsGAATTATT (RBP4) NP_001310447.1:p.Met1=
NM_001323518.2:c.3_10delinsGAATTATT (RBP4) NP_001310447.1:p.Met1=