Canonical Allele Identifier: CA352202943

Gene: CX3CR1

Linked Data

• COSMIC: COSM480079 ; COSM1137025
• MyVariant Identifiers: chr3:g.39307549A>G (hg19) ; chr3:g.39266058A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39266058A>G , CM000665.2:g.39266058A>G	GRCh38
NC_000003.11:g.39307549A>G , CM000665.1:g.39307549A>G	GRCh37
NC_000003.10:g.39282553A>G	NCBI36
NG_016362.1:g.20678T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.452T>C MANE Select	ENSP00000382166.3:p.Leu151Pro
ENST00000358309.3:c.548T>C	ENSP00000351059.3:p.Leu183Pro
ENST00000399220.2:c.452T>C	ENSP00000382166.2:p.Leu151Pro
ENST00000435290.1:c.452T>C	ENSP00000394960.1:p.Leu151Pro
ENST00000541347.5:c.452T>C	ENSP00000439140.1:p.Leu151Pro
ENST00000542107.5:c.452T>C	ENSP00000444928.1:p.Leu151Pro
NM_001171171.1:c.452T>C	NP_001164642.1:p.Leu151Pro
NM_001171172.1:c.452T>C	NP_001164643.1:p.Leu151Pro
NM_001171174.1:c.548T>C	NP_001164645.1:p.Leu183Pro
NM_001337.3:c.452T>C	NP_001328.1:p.Leu151Pro
NM_001337.4:c.452T>C MANE Select	NP_001328.1:p.Leu151Pro
NM_001171171.2:c.452T>C	NP_001164642.1:p.Leu151Pro
NM_001171172.2:c.452T>C	NP_001164643.1:p.Leu151Pro