Canonical Allele Identifier: CA1358882694
Gene: CX3CR1 HGNC NCBI

Linked Data

dbSNP Id: rs2040680603

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265364_39265366del , CM000665.2:g.39265364_39265366del GRCh38
NC_000003.11:g.39306855_39306857del , CM000665.1:g.39306855_39306857del GRCh37
NC_000003.10:g.39281859_39281861del NCBI36
NG_016362.1:g.21375_21377del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.*81_*83del MANE Select ENSP00000382166.3:n.*81_*83del
ENST00000358309.3:c.*81_*83del ENSP00000351059.3:n.*81_*83del
ENST00000399220.2:c.*81_*83del ENSP00000382166.2:n.*81_*83del
ENST00000541347.5:c.*81_*83del ENSP00000439140.1:n.*81_*83del
ENST00000542107.5:c.*81_*83del ENSP00000444928.1:n.*81_*83del
NM_001171171.1:c.*81_*83del NP_001164642.1:n.*81_*83del
NM_001171172.1:c.*81_*83del NP_001164643.1:n.*81_*83del
NM_001171174.1:c.*81_*83del NP_001164645.1:n.*81_*83del
NM_001337.3:c.*81_*83del NP_001328.1:n.*81_*83del
NM_001337.4:c.*81_*83del MANE Select NP_001328.1:n.*81_*83del
NM_001171171.2:c.*81_*83del NP_001164642.1:n.*81_*83del
NM_001171172.2:c.*81_*83del NP_001164643.1:n.*81_*83del