Canonical Allele Identifier: CA1928693817

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601731_93601732delinsAT , CM000672.2:g.93601731_93601732delinsAT GRCh38
NC_000010.10:g.95361488_95361489delinsAT , CM000672.1:g.95361488_95361489delinsAT GRCh37
NC_000010.9:g.95351478_95351479delinsAT NCBI36
NG_009104.1:g.4505_4506delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000371469.2:c.-16_-15delinsAT (RBP4) ENSP00000360524.2:n.-16_-15delinsAT
ENST00000604414.1:c.697-2343_697-2342delinsAT (FFAR4) ENSP00000474477.1:n.697-2343_697-2342deli...
NM_001323518.1:c.-16_-15delinsAT (RBP4) NP_001310447.1:n.-16_-15delinsAT
NM_001323518.2:c.-16_-15delinsAT (RBP4) NP_001310447.1:n.-16_-15delinsAT