Canonical Allele Identifier: CA2341531244
Community Standard Title: NM_002029.4(FPR1):c.32T= (p.Ile11=)
Gene: FPR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746963A= , CM000681.2:g.51746963A= GRCh38
NC_000019.9:g.52250216A= , CM000681.1:g.52250216A= GRCh37
NC_000019.8:g.56942028A= NCBI36
NG_023426.1:g.9935T= , LRG_146:g.9935T=

Transcript Alleles

HGVS Amino-acid Change
NM_002029.4:c.32T= MANE Select NP_002020.1:p.Ile11=
ENST00000304748.5:c.32T= MANE Select ENSP00000302707.3:p.Ile11=
NM_001193306.1:c.32T= NP_001180235.1:p.Ile11=
NM_001193306.2:c.32T= NP_001180235.1:p.Ile11=
NM_002029.3:c.32T= , LRG_146t1:c.32T= NP_002020.1:p.Ile11=
ENST00000304748.4:c.32T= ENSP00000302707.3:p.Ile11=
ENST00000594900.1:c.32T= ENSP00000470750.1:p.Ile11=
ENST00000594900.2:c.32T= ENSP00000470750.2:p.Ile11=
ENST00000595042.5:c.32T= ENSP00000471493.1:p.Ile11=
ENST00000600815.1:c.32T= ENSP00000472936.1:p.Ile11=
ENST00000600815.2:c.32T= ENSP00000472936.2:p.Ile11=