Canonical Allele Identifier: CA1358882801

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265649_39265652delinsGCAA , CM000665.2:g.39265649_39265652delinsGCAA	GRCh38
NC_000003.11:g.39307140_39307143delinsGCAA , CM000665.1:g.39307140_39307143delinsGCAA	GRCh37
NC_000003.10:g.39282144_39282147delinsGCAA	NCBI36
NG_016362.1:g.21084_21087delinsTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.858_861delinsTTGC MANE Select	ENSP00000382166.3:p.Cys286=
ENST00000358309.3:c.954_957delinsTTGC	ENSP00000351059.3:p.Cys318=
ENST00000399220.2:c.858_861delinsTTGC	ENSP00000382166.2:p.Cys286=
ENST00000541347.5:c.858_861delinsTTGC	ENSP00000439140.1:p.Cys286=
ENST00000542107.5:c.858_861delinsTTGC	ENSP00000444928.1:p.Cys286=
NM_001171171.1:c.858_861delinsTTGC	NP_001164642.1:p.Cys286=
NM_001171172.1:c.858_861delinsTTGC	NP_001164643.1:p.Cys286=
NM_001171174.1:c.954_957delinsTTGC	NP_001164645.1:p.Cys318=
NM_001337.3:c.858_861delinsTTGC	NP_001328.1:p.Cys286=
NM_001337.4:c.858_861delinsTTGC MANE Select	NP_001328.1:p.Cys286=
NM_001171171.2:c.858_861delinsTTGC	NP_001164642.1:p.Cys286=
NM_001171172.2:c.858_861delinsTTGC	NP_001164643.1:p.Cys286=