Canonical Allele Identifier: CA1358882746
Gene: CX3CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265508A= , CM000665.2:g.39265508A= GRCh38
NC_000003.11:g.39306999A= , CM000665.1:g.39306999A= GRCh37
NC_000003.10:g.39282003A= NCBI36
NG_016362.1:g.21228T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.1002T= MANE Select ENSP00000382166.3:p.His334=
ENST00000358309.3:c.1098T= ENSP00000351059.3:p.His366=
ENST00000399220.2:c.1002T= ENSP00000382166.2:p.His334=
ENST00000541347.5:c.1002T= ENSP00000439140.1:p.His334=
ENST00000542107.5:c.1002T= ENSP00000444928.1:p.His334=
NM_001171171.1:c.1002T= NP_001164642.1:p.His334=
NM_001171172.1:c.1002T= NP_001164643.1:p.His334=
NM_001171174.1:c.1098T= NP_001164645.1:p.His366=
NM_001337.3:c.1002T= NP_001328.1:p.His334=
NM_001337.4:c.1002T= MANE Select NP_001328.1:p.His334=
NM_001171171.2:c.1002T= NP_001164642.1:p.His334=
NM_001171172.2:c.1002T= NP_001164643.1:p.His334=