Canonical Allele Identifier: CA996919348
Gene: FPR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51746321_51746322insT , CM000681.2:g.51746321_51746322insT GRCh38
NC_000019.9:g.52249574_52249575insT , CM000681.1:g.52249574_52249575insT GRCh37
NC_000019.8:g.56941386_56941387insT NCBI36
NG_023426.1:g.10576_10577insA , LRG_146:g.10576_10577insA

Transcript Alleles

HGVS Amino-acid change
ENST00000594900.2:c.673_674insA ENSP00000470750.2:p.Ala225AspfsTer11
ENST00000600815.2:c.673_674insA ENSP00000472936.2:p.Ala225AspfsTer11
ENST00000304748.5:c.673_674insA MANE Select ENSP00000302707.3:p.Ala225AspfsTer11
ENST00000304748.4:c.673_674insA ENSP00000302707.3:p.Ala225AspfsTer11
ENST00000595042.5:c.673_674insA ENSP00000471493.1:p.Ala225AspfsTer11
NM_001193306.1:c.673_674insA NP_001180235.1:p.Ala225AspfsTer11
NM_002029.3:c.673_674insA , LRG_146t1:c.673_674insA NP_002020.1:p.Ala225AspfsTer11
NM_001193306.2:c.673_674insA NP_001180235.1:p.Ala225AspfsTer11
NM_002029.4:c.673_674insA MANE Select NP_002020.1:p.Ala225AspfsTer11