Canonical Allele Identifier: CA542616777

Gene: CX3CR1

Linked Data

• dbSNP Id: rs1465558098
• gnomAD v2: 3-39307155-T-TG
• gnomAD v4: 3-39265664-T-TG
• MyVariant Identifiers: chr3:g.39307155_39307156insG (hg19) ; chr3:g.39265664_39265665insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265665dup , CM000665.2:g.39265665dup	GRCh38
NC_000003.11:g.39307156dup , CM000665.1:g.39307156dup	GRCh37
NC_000003.10:g.39282160dup	NCBI36
NG_016362.1:g.21071dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.845dup MANE Select	ENSP00000382166.3:p.Phe283IlefsTer2
ENST00000358309.3:c.941dup	ENSP00000351059.3:p.Phe315IlefsTer2
ENST00000399220.2:c.845dup	ENSP00000382166.2:p.Phe283IlefsTer2
ENST00000541347.5:c.845dup	ENSP00000439140.1:p.Phe283IlefsTer2
ENST00000542107.5:c.845dup	ENSP00000444928.1:p.Phe283IlefsTer2
NM_001171171.1:c.845dup	NP_001164642.1:p.Phe283IlefsTer2
NM_001171172.1:c.845dup	NP_001164643.1:p.Phe283IlefsTer2
NM_001171174.1:c.941dup	NP_001164645.1:p.Phe315IlefsTer2
NM_001337.3:c.845dup	NP_001328.1:p.Phe283IlefsTer2
NM_001337.4:c.845dup MANE Select	NP_001328.1:p.Phe283IlefsTer2
NM_001171171.2:c.845dup	NP_001164642.1:p.Phe283IlefsTer2
NM_001171172.2:c.845dup	NP_001164643.1:p.Phe283IlefsTer2