Canonical Allele Identifier: CA9616405

Gene: FPR1

Linked Data

• dbSNP Id: rs775516421
• ExAC: 19:52249591 GAC / G
• gnomAD v2: 19-52249591-GAC-G
• gnomAD v4: 19-51746338-GAC-G
• MyVariant Identifiers: chr19:g.52249592_52249593del (hg19) ; chr19:g.51746339_51746340del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746340_51746341del , CM000681.2:g.51746340_51746341del	GRCh38
NC_000019.9:g.52249593_52249594del , CM000681.1:g.52249593_52249594del	GRCh37
NC_000019.8:g.56941405_56941406del	NCBI36
NG_023426.1:g.10558_10559del , LRG_146:g.10558_10559del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.655_656del	ENSP00000470750.2:p.Val219GlnfsTer16
ENST00000600815.2:c.655_656del	ENSP00000472936.2:p.Val219GlnfsTer16
ENST00000304748.5:c.655_656del MANE Select	ENSP00000302707.3:p.Val219GlnfsTer16
ENST00000304748.4:c.655_656del	ENSP00000302707.3:p.Val219GlnfsTer16
ENST00000595042.5:c.655_656del	ENSP00000471493.1:p.Val219GlnfsTer16
NM_001193306.1:c.655_656del	NP_001180235.1:p.Val219GlnfsTer16
NM_002029.3:c.655_656del , LRG_146t1:c.655_656del	NP_002020.1:p.Val219GlnfsTer16
NM_001193306.2:c.655_656del	NP_001180235.1:p.Val219GlnfsTer16
NM_002029.4:c.655_656del MANE Select	NP_002020.1:p.Val219GlnfsTer16