Canonical Allele Identifier: CA9616423
Gene: FPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746399G>A , CM000681.2:g.51746399G>A GRCh38
NC_000019.9:g.52249652G>A , CM000681.1:g.52249652G>A GRCh37
NC_000019.8:g.56941464G>A NCBI36
NG_023426.1:g.10499C>T , LRG_146:g.10499C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.596C>T ENSP00000470750.2:p.Thr199Met
ENST00000600815.2:c.596C>T ENSP00000472936.2:p.Thr199Met
ENST00000304748.5:c.596C>T MANE Select ENSP00000302707.3:p.Thr199Met
ENST00000304748.4:c.596C>T ENSP00000302707.3:p.Thr199Met
ENST00000595042.5:c.596C>T ENSP00000471493.1:p.Thr199Met
NM_001193306.1:c.596C>T NP_001180235.1:p.Thr199Met
NM_002029.3:c.596C>T , LRG_146t1:c.596C>T NP_002020.1:p.Thr199Met
NM_001193306.2:c.596C>T NP_001180235.1:p.Thr199Met
NM_002029.4:c.596C>T MANE Select NP_002020.1:p.Thr199Met