Canonical Allele Identifier: CA508815102

Gene: FPR1

Linked Data

• MyVariant Identifiers: chr19:g.52249579A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746326A>C , CM000681.2:g.51746326A>C	GRCh38
NC_000019.9:g.52249579A>C , CM000681.1:g.52249579A>C	GRCh37
NC_000019.8:g.56941391A>C	NCBI36
NG_023426.1:g.10572T>G , LRG_146:g.10572T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.669T>G	ENSP00000470750.2:p.Leu223=
ENST00000600815.2:c.669T>G	ENSP00000472936.2:p.Leu223=
ENST00000304748.5:c.669T>G MANE Select	ENSP00000302707.3:p.Leu223=
ENST00000304748.4:c.669T>G	ENSP00000302707.3:p.Leu223=
ENST00000595042.5:c.669T>G	ENSP00000471493.1:p.Leu223=
NM_001193306.1:c.669T>G	NP_001180235.1:p.Leu223=
NM_002029.3:c.669T>G , LRG_146t1:c.669T>G	NP_002020.1:p.Leu223=
NM_001193306.2:c.669T>G	NP_001180235.1:p.Leu223=
NM_002029.4:c.669T>G MANE Select	NP_002020.1:p.Leu223=