Canonical Allele Identifier: CA9616476

Gene: FPR1

Linked Data

• dbSNP Id: rs764598916
• ExAC: 19:52249873 AAC / A
• gnomAD v2: 19-52249873-AAC-A
• gnomAD v3: 19-51746620-AAC-A
• gnomAD v4: 19-51746620-AAC-A
• MyVariant Identifiers: chr19:g.52249874_52249875del (hg19) ; chr19:g.51746621_51746622del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746624_51746625del , CM000681.2:g.51746624_51746625del	GRCh38
NC_000019.9:g.52249877_52249878del , CM000681.1:g.52249877_52249878del	GRCh37
NC_000019.8:g.56941689_56941690del	NCBI36
NG_023426.1:g.10276_10277del , LRG_146:g.10276_10277del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.373_374del	ENSP00000470750.2:p.Val125LeufsTer?
ENST00000600815.2:c.373_374del	ENSP00000472936.2:p.Val125LeufsTer?
ENST00000304748.5:c.373_374del MANE Select	ENSP00000302707.3:p.Val125LeufsTer?
ENST00000304748.4:c.373_374del	ENSP00000302707.3:p.Val125LeufsTer?
ENST00000595042.5:c.373_374del	ENSP00000471493.1:p.Val125LeufsTer?
ENST00000600815.1:c.373_374del	ENSP00000472936.1:p.Val125LeufsTer?
NM_001193306.1:c.373_374del	NP_001180235.1:p.Val125LeufsTer?
NM_002029.3:c.373_374del , LRG_146t1:c.373_374del	NP_002020.1:p.Val125LeufsTer?
NM_001193306.2:c.373_374del	NP_001180235.1:p.Val125LeufsTer?
NM_002029.4:c.373_374del MANE Select	NP_002020.1:p.Val125LeufsTer?