Canonical Allele Identifier: CA407116357
Gene: FPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746174C>G , CM000681.2:g.51746174C>G GRCh38
NC_000019.9:g.52249427C>G , CM000681.1:g.52249427C>G GRCh37
NC_000019.8:g.56941239C>G NCBI36
NG_023426.1:g.10724G>C , LRG_146:g.10724G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.821G>C ENSP00000470750.2:p.Gly274Ala
ENST00000600815.2:c.821G>C ENSP00000472936.2:p.Gly274Ala
ENST00000304748.5:c.821G>C MANE Select ENSP00000302707.3:p.Gly274Ala
ENST00000304748.4:c.821G>C ENSP00000302707.3:p.Gly274Ala
ENST00000595042.5:c.821G>C ENSP00000471493.1:p.Gly274Ala
NM_001193306.1:c.821G>C NP_001180235.1:p.Gly274Ala
NM_002029.3:c.821G>C , LRG_146t1:c.821G>C NP_002020.1:p.Gly274Ala
NM_001193306.2:c.821G>C NP_001180235.1:p.Gly274Ala
NM_002029.4:c.821G>C MANE Select NP_002020.1:p.Gly274Ala