Canonical Allele Identifier: CA352200247

Gene: CX3CR1

Linked Data

• MyVariant Identifiers: chr3:g.39307171A>G (hg19) ; chr3:g.39265680A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265680A>G , CM000665.2:g.39265680A>G	GRCh38
NC_000003.11:g.39307171A>G , CM000665.1:g.39307171A>G	GRCh37
NC_000003.10:g.39282175A>G	NCBI36
NG_016362.1:g.21056T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.830T>C MANE Select	ENSP00000382166.3:p.Val277Ala
ENST00000358309.3:c.926T>C	ENSP00000351059.3:p.Val309Ala
ENST00000399220.2:c.830T>C	ENSP00000382166.2:p.Val277Ala
ENST00000541347.5:c.830T>C	ENSP00000439140.1:p.Val277Ala
ENST00000542107.5:c.830T>C	ENSP00000444928.1:p.Val277Ala
NM_001171171.1:c.830T>C	NP_001164642.1:p.Val277Ala
NM_001171172.1:c.830T>C	NP_001164643.1:p.Val277Ala
NM_001171174.1:c.926T>C	NP_001164645.1:p.Val309Ala
NM_001337.3:c.830T>C	NP_001328.1:p.Val277Ala
NM_001337.4:c.830T>C MANE Select	NP_001328.1:p.Val277Ala
NM_001171171.2:c.830T>C	NP_001164642.1:p.Val277Ala
NM_001171172.2:c.830T>C	NP_001164643.1:p.Val277Ala