Canonical Allele Identifier: CA1358882940

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39266009_39266010delinsGA , CM000665.2:g.39266009_39266010delinsGA	GRCh38
NC_000003.11:g.39307500_39307501delinsGA , CM000665.1:g.39307500_39307501delinsGA	GRCh37
NC_000003.10:g.39282504_39282505delinsGA	NCBI36
NG_016362.1:g.20726_20727delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.500_501delinsTC MANE Select	ENSP00000382166.3:p.Phe167=
ENST00000358309.3:c.596_597delinsTC	ENSP00000351059.3:p.Phe199=
ENST00000399220.2:c.500_501delinsTC	ENSP00000382166.2:p.Phe167=
ENST00000541347.5:c.500_501delinsTC	ENSP00000439140.1:p.Phe167=
ENST00000542107.5:c.500_501delinsTC	ENSP00000444928.1:p.Phe167=
NM_001171171.1:c.500_501delinsTC	NP_001164642.1:p.Phe167=
NM_001171172.1:c.500_501delinsTC	NP_001164643.1:p.Phe167=
NM_001171174.1:c.596_597delinsTC	NP_001164645.1:p.Phe199=
NM_001337.3:c.500_501delinsTC	NP_001328.1:p.Phe167=
NM_001337.4:c.500_501delinsTC MANE Select	NP_001328.1:p.Phe167=
NM_001171171.2:c.500_501delinsTC	NP_001164642.1:p.Phe167=
NM_001171172.2:c.500_501delinsTC	NP_001164643.1:p.Phe167=