Canonical Allele Identifier: CA1928693849
Gene: FFAR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601755_93601759delinsCTCTT , CM000672.2:g.93601755_93601759delinsCTCTT GRCh38
NC_000010.10:g.95361512_95361516delinsCTCTT , CM000672.1:g.95361512_95361516delinsCTCTT GRCh37
NC_000010.9:g.95351502_95351506delinsCTCTT NCBI36
NG_009104.1:g.4478_4482delinsAAGAG

Transcript Alleles

HGVS Amino-acid change
ENST00000604414.1:c.697-2319_697-2315delinsCTCTT ENSP00000474477.1:n.697-2319_697-2315deli...