Canonical Allele Identifier: CA211550505

Gene: RBP4 FFAR4

Linked Data

• dbSNP Id: rs36035572
• gnomAD v2: 10-95353242-CA-C
• gnomAD v3: 10-93593485-CA-C
• gnomAD v4: 10-93593485-CA-C
• MyVariant Identifiers: chr10:g.95353243del (hg19) ; chr10:g.93593486del (hg38)

Genomic Alleles

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

Transcript Alleles

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