Canonical Allele Identifier: CA9616458
Gene: FPR1 HGNC NCBI

Linked Data

dbSNP Id: rs763517926

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746530del , CM000681.2:g.51746530del GRCh38
NC_000019.9:g.52249783del , CM000681.1:g.52249783del GRCh37
NC_000019.8:g.56941595del NCBI36
NG_023426.1:g.10369del , LRG_146:g.10369del

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.466del ENSP00000470750.2:p.Leu156SerfsTer9
ENST00000600815.2:c.466del ENSP00000472936.2:p.Leu156SerfsTer9
ENST00000304748.5:c.466del MANE Select ENSP00000302707.3:p.Leu156SerfsTer9
ENST00000304748.4:c.466del ENSP00000302707.3:p.Leu156SerfsTer9
ENST00000595042.5:c.466del ENSP00000471493.1:p.Leu156SerfsTer9
ENST00000600815.1:c.466del ENSP00000472936.1:p.Leu156SerfsTer9
NM_001193306.1:c.466del NP_001180235.1:p.Leu156SerfsTer9
NM_002029.3:c.466del , LRG_146t1:c.466del NP_002020.1:p.Leu156SerfsTer9
NM_001193306.2:c.466del NP_001180235.1:p.Leu156SerfsTer9
NM_002029.4:c.466del MANE Select NP_002020.1:p.Leu156SerfsTer9