Canonical Allele Identifier: CA407117684

Gene: FPR1

Linked Data

• ClinVar Variation Id: 2820782
• ClinVar RCV Id: RCV003762520
• MyVariant Identifiers: chr19:g.52249606C>T (hg19) ; chr19:g.51746353C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51746353C>T , CM000681.2:g.51746353C>T	GRCh38
NC_000019.9:g.52249606C>T , CM000681.1:g.52249606C>T	GRCh37
NC_000019.8:g.56941418C>T	NCBI36
NG_023426.1:g.10545G>A , LRG_146:g.10545G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594900.2:c.642G>A	ENSP00000470750.2:p.Met214Ile
ENST00000600815.2:c.642G>A	ENSP00000472936.2:p.Met214Ile
ENST00000304748.5:c.642G>A MANE Select	ENSP00000302707.3:p.Met214Ile
ENST00000304748.4:c.642G>A	ENSP00000302707.3:p.Met214Ile
ENST00000595042.5:c.642G>A	ENSP00000471493.1:p.Met214Ile
NM_001193306.1:c.642G>A	NP_001180235.1:p.Met214Ile
NM_002029.3:c.642G>A , LRG_146t1:c.642G>A	NP_002020.1:p.Met214Ile
NM_001193306.2:c.642G>A	NP_001180235.1:p.Met214Ile
NM_002029.4:c.642G>A MANE Select	NP_002020.1:p.Met214Ile