Canonical Allele Identifier: CA1358882829

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265722G= , CM000665.2:g.39265722G=	GRCh38
NC_000003.11:g.39307213G= , CM000665.1:g.39307213G=	GRCh37
NC_000003.10:g.39282217G=	NCBI36
NG_016362.1:g.21014C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.788C= MANE Select	ENSP00000382166.3:p.Pro263=
ENST00000358309.3:c.884C=	ENSP00000351059.3:p.Pro295=
ENST00000399220.2:c.788C=	ENSP00000382166.2:p.Pro263=
ENST00000541347.5:c.788C=	ENSP00000439140.1:p.Pro263=
ENST00000542107.5:c.788C=	ENSP00000444928.1:p.Pro263=
NM_001171171.1:c.788C=	NP_001164642.1:p.Pro263=
NM_001171172.1:c.788C=	NP_001164643.1:p.Pro263=
NM_001171174.1:c.884C=	NP_001164645.1:p.Pro295=
NM_001337.3:c.788C=	NP_001328.1:p.Pro263=
NM_001337.4:c.788C= MANE Select	NP_001328.1:p.Pro263=
NM_001171171.2:c.788C=	NP_001164642.1:p.Pro263=
NM_001171172.2:c.788C=	NP_001164643.1:p.Pro263=