Canonical Allele Identifier: CA2566406710

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39266031_39266032insTTTTGGTGG , CM000665.2:g.39266031_39266032insTTTTGGTGG	GRCh38
NC_000003.11:g.39307522_39307523insTTTTGGTGG , CM000665.1:g.39307522_39307523insTTTTGGTGG	GRCh37
NC_000003.10:g.39282526_39282527insTTTTGGTGG	NCBI36
NG_016362.1:g.20704_20705insCCACCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.478_479insCCACCAAAA MANE Select	ENSP00000382166.3:p.Val160delinsAlaThrLysMet
ENST00000358309.3:c.574_575insCCACCAAAA	ENSP00000351059.3:p.Val192delinsAlaThrLysMet
ENST00000399220.2:c.478_479insCCACCAAAA	ENSP00000382166.2:p.Val160delinsAlaThrLysMet
ENST00000435290.1:c.478_479insCCACCAAAA	ENSP00000394960.1:p.Val160delinsAlaThrLysMet
ENST00000541347.5:c.478_479insCCACCAAAA	ENSP00000439140.1:p.Val160delinsAlaThrLysMet
ENST00000542107.5:c.478_479insCCACCAAAA	ENSP00000444928.1:p.Val160delinsAlaThrLysMet
NM_001171171.1:c.478_479insCCACCAAAA	NP_001164642.1:p.Val160delinsAlaThrLysMet
NM_001171172.1:c.478_479insCCACCAAAA	NP_001164643.1:p.Val160delinsAlaThrLysMet
NM_001171174.1:c.574_575insCCACCAAAA	NP_001164645.1:p.Val192delinsAlaThrLysMet
NM_001337.3:c.478_479insCCACCAAAA	NP_001328.1:p.Val160delinsAlaThrLysMet
NM_001337.4:c.478_479insCCACCAAAA MANE Select	NP_001328.1:p.Val160delinsAlaThrLysMet
NM_001171171.2:c.478_479insCCACCAAAA	NP_001164642.1:p.Val160delinsAlaThrLysMet
NM_001171172.2:c.478_479insCCACCAAAA	NP_001164643.1:p.Val160delinsAlaThrLysMet