Canonical Allele Identifier: CA352200193
Gene: CX3CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265671G>C , CM000665.2:g.39265671G>C GRCh38
NC_000003.11:g.39307162G>C , CM000665.1:g.39307162G>C GRCh37
NC_000003.10:g.39282166G>C NCBI36
NG_016362.1:g.21065C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399220.3:c.839C>G MANE Select ENSP00000382166.3:p.Thr280Arg
ENST00000358309.3:c.935C>G ENSP00000351059.3:p.Thr312Arg
ENST00000399220.2:c.839C>G ENSP00000382166.2:p.Thr280Arg
ENST00000541347.5:c.839C>G ENSP00000439140.1:p.Thr280Arg
ENST00000542107.5:c.839C>G ENSP00000444928.1:p.Thr280Arg
NM_001171171.1:c.839C>G NP_001164642.1:p.Thr280Arg
NM_001171172.1:c.839C>G NP_001164643.1:p.Thr280Arg
NM_001171174.1:c.935C>G NP_001164645.1:p.Thr312Arg
NM_001337.3:c.839C>G NP_001328.1:p.Thr280Arg
NM_001337.4:c.839C>G MANE Select NP_001328.1:p.Thr280Arg
NM_001171171.2:c.839C>G NP_001164642.1:p.Thr280Arg
NM_001171172.2:c.839C>G NP_001164643.1:p.Thr280Arg