Canonical Allele Identifier: CA352202656

Gene: CX3CR1

Linked Data

• MyVariant Identifiers: chr3:g.39307502A>T (hg19) ; chr3:g.39266011A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39266011A>T , CM000665.2:g.39266011A>T	GRCh38
NC_000003.11:g.39307502A>T , CM000665.1:g.39307502A>T	GRCh37
NC_000003.10:g.39282506A>T	NCBI36
NG_016362.1:g.20725T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.499T>A MANE Select	ENSP00000382166.3:p.Phe167Ile
ENST00000358309.3:c.595T>A	ENSP00000351059.3:p.Phe199Ile
ENST00000399220.2:c.499T>A	ENSP00000382166.2:p.Phe167Ile
ENST00000435290.1:c.499T>A
ENST00000541347.5:c.499T>A	ENSP00000439140.1:p.Phe167Ile
ENST00000542107.5:c.499T>A	ENSP00000444928.1:p.Phe167Ile
NM_001171171.1:c.499T>A	NP_001164642.1:p.Phe167Ile
NM_001171172.1:c.499T>A	NP_001164643.1:p.Phe167Ile
NM_001171174.1:c.595T>A	NP_001164645.1:p.Phe199Ile
NM_001337.3:c.499T>A	NP_001328.1:p.Phe167Ile
NM_001337.4:c.499T>A MANE Select	NP_001328.1:p.Phe167Ile
NM_001171171.2:c.499T>A	NP_001164642.1:p.Phe167Ile
NM_001171172.2:c.499T>A	NP_001164643.1:p.Phe167Ile