Canonical Allele Identifier: CA031269
Gene: CX3CR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8152

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.[39265671G>A;39265765C>T] , CM000665.2:g.[39265671G>A;39265765C>T] GRCh38
NC_000003.11:g.[39307162G>A;39307256C>T] , CM000665.1:g.[39307162G>A;39307256C>T] GRCh37
NC_000003.10:g.[39282166G>A;39282260C>T] NCBI36
NG_016362.1:g.[20971G>A;21065C>T]

Transcript Alleles

HGVS Amino-acid change
ENST00000399220.3:c.[745G>A;839C>T] MANE Select ENSP00000382166.3:p.[Val249Ile;Thr280Met]...
ENST00000358309.3:c.[841G>A;935C>T] ENSP00000351059.3:p.[Val281Ile;Thr312Met]...
ENST00000399220.2:c.[745G>A;839C>T] ENSP00000382166.2:p.[Val249Ile;Thr280Met]...
ENST00000541347.5:c.[745G>A;839C>T] ENSP00000439140.1:p.[Val249Ile;Thr280Met]...
ENST00000542107.5:c.[745G>A;839C>T] ENSP00000444928.1:p.[Val249Ile;Thr280Met]...
NM_001171171.1:c.[745G>A;839C>T] NP_001164642.1:p.[Val249Ile;Thr280Met]
NM_001171172.1:c.[745G>A;839C>T] NP_001164643.1:p.[Val249Ile;Thr280Met]
NM_001171174.1:c.[841G>A;935C>T] NP_001164645.1:p.[Val281Ile;Thr312Met]
NM_001337.3:c.[745G>A;839C>T] NP_001328.1:p.[Val249Ile;Thr280Met]
NM_001337.4:c.[745G>A;839C>T] MANE Select NP_001328.1:p.[Val249Ile;Thr280Met]
NM_001171171.2:c.[745G>A;839C>T] NP_001164642.1:p.[Val249Ile;Thr280Met]
NM_001171172.2:c.[745G>A;839C>T] NP_001164643.1:p.[Val249Ile;Thr280Met]