Canonical Allele Identifier: CA1358882777

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265582_39265583delinsTC , CM000665.2:g.39265582_39265583delinsTC	GRCh38
NC_000003.11:g.39307073_39307074delinsTC , CM000665.1:g.39307073_39307074delinsTC	GRCh37
NC_000003.10:g.39282077_39282078delinsTC	NCBI36
NG_016362.1:g.21153_21154delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.927_928delinsGA MANE Select	ENSP00000382166.3:p.Gly309=
ENST00000358309.3:c.1023_1024delinsGA	ENSP00000351059.3:p.Gly341=
ENST00000399220.2:c.927_928delinsGA	ENSP00000382166.2:p.Gly309=
ENST00000541347.5:c.927_928delinsGA	ENSP00000439140.1:p.Gly309=
ENST00000542107.5:c.927_928delinsGA	ENSP00000444928.1:p.Gly309=
NM_001171171.1:c.927_928delinsGA	NP_001164642.1:p.Gly309=
NM_001171172.1:c.927_928delinsGA	NP_001164643.1:p.Gly309=
NM_001171174.1:c.1023_1024delinsGA	NP_001164645.1:p.Gly341=
NM_001337.3:c.927_928delinsGA	NP_001328.1:p.Gly309=
NM_001337.4:c.927_928delinsGA MANE Select	NP_001328.1:p.Gly309=
NM_001171171.2:c.927_928delinsGA	NP_001164642.1:p.Gly309=
NM_001171172.2:c.927_928delinsGA	NP_001164643.1:p.Gly309=