Canonical Allele Identifier: CA352200996

Gene: CX3CR1

Linked Data

• MyVariant Identifiers: chr3:g.39307267G>C (hg19) ; chr3:g.39265776G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265776G>C , CM000665.2:g.39265776G>C	GRCh38
NC_000003.11:g.39307267G>C , CM000665.1:g.39307267G>C	GRCh37
NC_000003.10:g.39282271G>C	NCBI36
NG_016362.1:g.20960C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.734C>G MANE Select	ENSP00000382166.3:p.Thr245Arg
ENST00000358309.3:c.830C>G	ENSP00000351059.3:p.Thr277Arg
ENST00000399220.2:c.734C>G	ENSP00000382166.2:p.Thr245Arg
ENST00000541347.5:c.734C>G	ENSP00000439140.1:p.Thr245Arg
ENST00000542107.5:c.734C>G	ENSP00000444928.1:p.Thr245Arg
NM_001171171.1:c.734C>G	NP_001164642.1:p.Thr245Arg
NM_001171172.1:c.734C>G	NP_001164643.1:p.Thr245Arg
NM_001171174.1:c.830C>G	NP_001164645.1:p.Thr277Arg
NM_001337.3:c.734C>G	NP_001328.1:p.Thr245Arg
NM_001337.4:c.734C>G MANE Select	NP_001328.1:p.Thr245Arg
NM_001171171.2:c.734C>G	NP_001164642.1:p.Thr245Arg
NM_001171172.2:c.734C>G	NP_001164643.1:p.Thr245Arg