Canonical Allele Identifier: CA595272839
Gene: RBP4 HGNC NCBI
FFAR4 HGNC NCBI

Linked Data

dbSNP Id: rs1406556944
gnomAD v2: 10-95361461-TGGAATAATTC-T
gnomAD v4: 10-93601704-TGGAATAATTC-T
MyVariant Identifiers: chr10:g.95361462_95361471del (hg19) chr10:g.93601705_93601714del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93601705_93601714del , CM000672.2:g.93601705_93601714del GRCh38
NC_000010.10:g.95361462_95361471del , CM000672.1:g.95361462_95361471del GRCh37
NC_000010.9:g.95351452_95351461del NCBI36
NG_009104.1:g.4523_4532del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371469.2:c.3_12del (RBP4) ENSP00000360524.2:p.Met1IlefsTer19
ENST00000604414.1:c.697-2369_697-2360del (FFAR4) ENSP00000474477.1:n.697-2369_697-2360del
ENST00000629763.2:c.3_12del (RBP4) ENSP00000487033.1:p.Met1IlefsTer19
NM_001323518.1:c.3_12del (RBP4) NP_001310447.1:p.Met1IlefsTer19
NM_001323518.2:c.3_12del (RBP4) NP_001310447.1:p.Met1IlefsTer19
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