Canonical Allele Identifier: CA658799307
Gene: FPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51745957_51745958delinsTG , CM000681.2:g.51745957_51745958delinsTG GRCh38
NC_000019.9:g.52249210_52249211delinsTG , CM000681.1:g.52249210_52249211delinsTG GRCh37
NC_000019.8:g.56941022_56941023delinsTG NCBI36
NG_023426.1:g.10940_10941delinsCA , LRG_146:g.10940_10941delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.1037_1038delinsCA ENSP00000470750.2:p.Glu346Ala
ENST00000600815.2:c.1037_1038delinsCA ENSP00000472936.2:p.Glu346Ala
ENST00000304748.5:c.1037_1038delinsCA MANE Select ENSP00000302707.3:p.Glu346Ala
ENST00000304748.4:c.1037_1038delinsCA ENSP00000302707.3:p.Glu346Ala
ENST00000595042.5:c.1037_1038delinsCA ENSP00000471493.1:p.Glu346Ala
NM_001193306.1:c.1037_1038delinsCA NP_001180235.1:p.Glu346Ala
NM_002029.3:c.1037_1038delinsCA , LRG_146t1:c.1037_1038delinsCA NP_002020.1:p.Glu346Ala
NM_001193306.2:c.1037_1038delinsCA NP_001180235.1:p.Glu346Ala
NM_002029.4:c.1037_1038delinsCA MANE Select NP_002020.1:p.Glu346Ala