Canonical Allele Identifier: CA1362034394

Gene: CCR3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46264639G= , CM000665.2:g.46264639G=	GRCh38
NC_000003.11:g.46306130G= , CM000665.1:g.46306130G=	GRCh37
NC_000003.10:g.46281134G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_178329.3:c.-11-509G= MANE Select	NP_847899.1:n.-11-509G=
ENST00000395940.3:c.-11-509G= MANE Select	ENSP00000379271.2:n.-11-509G=
NM_001164680.1:c.43+193G=	NP_001158152.1:n.43+193G=
NM_001164680.2:c.43+193G=	NP_001158152.1:n.43+193G=
NM_001837.3:c.-11-509G=	NP_001828.1:n.-11-509G=
NM_001837.4:c.-11-509G=	NP_001828.1:n.-11-509G=
NM_178328.1:c.52+184G=	NP_847898.1:n.52+184G=
NM_178329.2:c.-11-509G=	NP_847899.1:n.-11-509G=
ENST00000357422.2:c.-11-509G=	ENSP00000350003.2:n.-11-509G=
ENST00000395940.2:c.-11-509G=	ENSP00000379271.2:n.-11-509G=
ENST00000452454.1:c.-12+184G=	ENSP00000389336.1:n.-12+184G=
ENST00000457243.1:c.-12+193G=	ENSP00000401822.1:n.-12+193G=
ENST00000475150.1:n.1066+184G=
ENST00000484025.5:n.331G=
ENST00000545097.1:c.52+184G=	ENSP00000441600.1:n.52+184G=
XM_006712960.2:c.-11-509G=	XP_006713023.1:n.-11-509G=
XM_006712960.3:c.-11-509G=	XP_006713023.1:n.-11-509G=
XM_011533334.1:c.52+184G=	XP_011531636.1:n.52+184G=
XM_011533335.1:c.-11-509G=	XP_011531637.1:n.-11-509G=
XM_011533335.2:c.-11-509G=	XP_011531637.1:n.-11-509G=
XM_017005685.1:c.154+184G=	XP_016861174.1:n.154+184G=
XM_017005686.1:c.154+184G=	XP_016861175.1:n.154+184G=