Canonical Allele Identifier: CA14692192

Gene: FPR3 ZNF577

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51820963G>A , CM000681.2:g.51820963G>A	GRCh38
NC_000019.9:g.52324216G>A , CM000681.1:g.52324216G>A	GRCh37
NC_000019.8:g.57016028G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339223.5:c.-10-2776G>A (FPR3) MANE Select	ENSP00000341821.3:n.-10-2776G>A
ENST00000638827.1:c.*600-9289C>T (ZNF577)	ENSP00000492704.1:n.*600-9289C>T
ENST00000339223.4:c.-10-2776G>A (FPR3)	ENSP00000341821.3:n.-10-2776G>A
ENST00000595991.1:c.-10-2776G>A (FPR3)	ENSP00000470471.1:n.-10-2776G>A
NM_002030.3:c.-10-2776G>A (FPR3)	NP_002021.3:n.-10-2776G>A
XM_011526687.1:c.-10-2776G>A (FPR3)	XP_011524989.1:n.-10-2776G>A
XR_244009.2:n.653-6986C>T
NM_002030.4:c.-10-2776G>A (FPR3)	NP_002021.3:n.-10-2776G>A
XM_011526687.2:c.-10-2776G>A (FPR3)	XP_011524989.1:n.-10-2776G>A
XR_001753986.1:n.2465-6986C>T
XR_001753987.1:n.2470-6986C>T
XR_001753988.1:n.2291-6986C>T
XR_001753989.1:n.1718-6986C>T
XR_001753990.1:n.1544-6986C>T
XR_244009.3:n.653-6986C>T
NM_002030.5:c.-10-2776G>A (FPR3) MANE Select	NP_002021.3:n.-10-2776G>A
NR_163433.1:n.2153-6986C>T (ZNF577)