Canonical Allele Identifier: CA1358882670

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265307T= , CM000665.2:g.39265307T=	GRCh38
NC_000003.11:g.39306798T= , CM000665.1:g.39306798T=	GRCh37
NC_000003.10:g.39281802T=	NCBI36
NG_016362.1:g.21429A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.*135A= MANE Select	ENSP00000382166.3:n.*135A=
ENST00000358309.3:c.*135A=	ENSP00000351059.3:n.*135A=
ENST00000399220.2:c.*135A=	ENSP00000382166.2:n.*135A=
ENST00000541347.5:c.*135A=	ENSP00000439140.1:n.*135A=
ENST00000542107.5:c.*135A=	ENSP00000444928.1:n.*135A=
NM_001171171.1:c.*135A=	NP_001164642.1:n.*135A=
NM_001171172.1:c.*135A=	NP_001164643.1:n.*135A=
NM_001171174.1:c.*135A=	NP_001164645.1:n.*135A=
NM_001337.3:c.*135A=	NP_001328.1:n.*135A=
NM_001337.4:c.*135A= MANE Select	NP_001328.1:n.*135A=
NM_001171171.2:c.*135A=	NP_001164642.1:n.*135A=
NM_001171172.2:c.*135A=	NP_001164643.1:n.*135A=