Canonical Allele Identifier: CA2341530960
Gene: FPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746482C= , CM000681.2:g.51746482C= GRCh38
NC_000019.9:g.52249735C= , CM000681.1:g.52249735C= GRCh37
NC_000019.8:g.56941547C= NCBI36
NG_023426.1:g.10416G= , LRG_146:g.10416G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000594900.2:c.513G= ENSP00000470750.2:p.Thr171=
ENST00000600815.2:c.513G= ENSP00000472936.2:p.Thr171=
ENST00000304748.5:c.513G= MANE Select ENSP00000302707.3:p.Thr171=
ENST00000304748.4:c.513G= ENSP00000302707.3:p.Thr171=
ENST00000595042.5:c.513G= ENSP00000471493.1:p.Thr171=
ENST00000600815.1:c.513G= ENSP00000472936.1:p.Thr171=
NM_001193306.1:c.513G= NP_001180235.1:p.Thr171=
NM_002029.3:c.513G= , LRG_146t1:c.513G= NP_002020.1:p.Thr171=
NM_001193306.2:c.513G= NP_001180235.1:p.Thr171=
NM_002029.4:c.513G= MANE Select NP_002020.1:p.Thr171=