Canonical Allele Identifier: CA2665159117
Gene: CX3CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265626_39265627del , CM000665.2:g.39265626_39265627del GRCh38
NC_000003.11:g.39307117_39307118del , CM000665.1:g.39307117_39307118del GRCh37
NC_000003.10:g.39282121_39282122del NCBI36
NG_016362.1:g.21110_21111del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.884_885del MANE Select ENSP00000382166.3:p.Phe295CysfsTer28
ENST00000358309.3:c.980_981del ENSP00000351059.3:p.Phe327CysfsTer28
ENST00000399220.2:c.884_885del ENSP00000382166.2:p.Phe295CysfsTer28
ENST00000541347.5:c.884_885del ENSP00000439140.1:p.Phe295CysfsTer28
ENST00000542107.5:c.884_885del ENSP00000444928.1:p.Phe295CysfsTer28
NM_001171171.1:c.884_885del NP_001164642.1:p.Phe295CysfsTer28
NM_001171172.1:c.884_885del NP_001164643.1:p.Phe295CysfsTer28
NM_001171174.1:c.980_981del NP_001164645.1:p.Phe327CysfsTer28
NM_001337.3:c.884_885del NP_001328.1:p.Phe295CysfsTer28
NM_001337.4:c.884_885del MANE Select NP_001328.1:p.Phe295CysfsTer28
NM_001171171.2:c.884_885del NP_001164642.1:p.Phe295CysfsTer28
NM_001171172.2:c.884_885del NP_001164643.1:p.Phe295CysfsTer28