Canonical Allele Identifier: CA352198978
Gene: CX3CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265470C>G , CM000665.2:g.39265470C>G GRCh38
NC_000003.11:g.39306961C>G , CM000665.1:g.39306961C>G GRCh37
NC_000003.10:g.39281965C>G NCBI36
NG_016362.1:g.21266G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.1040G>C MANE Select ENSP00000382166.3:p.Ser347Thr
ENST00000358309.3:c.1136G>C ENSP00000351059.3:p.Ser379Thr
ENST00000399220.2:c.1040G>C ENSP00000382166.2:p.Ser347Thr
ENST00000541347.5:c.1040G>C ENSP00000439140.1:p.Ser347Thr
ENST00000542107.5:c.1040G>C ENSP00000444928.1:p.Ser347Thr
NM_001171171.1:c.1040G>C NP_001164642.1:p.Ser347Thr
NM_001171172.1:c.1040G>C NP_001164643.1:p.Ser347Thr
NM_001171174.1:c.1136G>C NP_001164645.1:p.Ser379Thr
NM_001337.3:c.1040G>C NP_001328.1:p.Ser347Thr
NM_001337.4:c.1040G>C MANE Select NP_001328.1:p.Ser347Thr
NM_001171171.2:c.1040G>C NP_001164642.1:p.Ser347Thr
NM_001171172.2:c.1040G>C NP_001164643.1:p.Ser347Thr