Canonical Allele Identifier: CA1358882625
Gene: CX3CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265184T= , CM000665.2:g.39265184T= GRCh38
NC_000003.11:g.39306675T= , CM000665.1:g.39306675T= GRCh37
NC_000003.10:g.39281679T= NCBI36
NG_016362.1:g.21552A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.*258A= MANE Select ENSP00000382166.3:n.*258A=
ENST00000358309.3:c.*258A= ENSP00000351059.3:n.*258A=
ENST00000399220.2:c.*258A= ENSP00000382166.2:n.*258A=
ENST00000541347.5:c.*258A= ENSP00000439140.1:n.*258A=
ENST00000542107.5:c.*258A= ENSP00000444928.1:n.*258A=
NM_001171171.1:c.*258A= NP_001164642.1:n.*258A=
NM_001171172.1:c.*258A= NP_001164643.1:n.*258A=
NM_001171174.1:c.*258A= NP_001164645.1:n.*258A=
NM_001337.3:c.*258A= NP_001328.1:n.*258A=
NM_001337.4:c.*258A= MANE Select NP_001328.1:n.*258A=
NM_001171171.2:c.*258A= NP_001164642.1:n.*258A=
NM_001171172.2:c.*258A= NP_001164643.1:n.*258A=