Canonical Allele Identifier: CA1358882795
Gene: CX3CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265634G= , CM000665.2:g.39265634G= GRCh38
NC_000003.11:g.39307125G= , CM000665.1:g.39307125G= GRCh37
NC_000003.10:g.39282129G= NCBI36
NG_016362.1:g.21102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.876C= MANE Select ENSP00000382166.3:p.Ile292=
ENST00000358309.3:c.972C= ENSP00000351059.3:p.Ile324=
ENST00000399220.2:c.876C= ENSP00000382166.2:p.Ile292=
ENST00000541347.5:c.876C= ENSP00000439140.1:p.Ile292=
ENST00000542107.5:c.876C= ENSP00000444928.1:p.Ile292=
NM_001171171.1:c.876C= NP_001164642.1:p.Ile292=
NM_001171172.1:c.876C= NP_001164643.1:p.Ile292=
NM_001171174.1:c.972C= NP_001164645.1:p.Ile324=
NM_001337.3:c.876C= NP_001328.1:p.Ile292=
NM_001337.4:c.876C= MANE Select NP_001328.1:p.Ile292=
NM_001171171.2:c.876C= NP_001164642.1:p.Ile292=
NM_001171172.2:c.876C= NP_001164643.1:p.Ile292=