Canonical Allele Identifier: CA1358882778
Gene: CX3CR1 HGNC NCBI

Linked Data

dbSNP Id: rs2040684140

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265585del , CM000665.2:g.39265585del GRCh38
NC_000003.11:g.39307076del , CM000665.1:g.39307076del GRCh37
NC_000003.10:g.39282080del NCBI36
NG_016362.1:g.21153del

Transcript Alleles

HGVS Amino-acid change
ENST00000399220.3:c.927del MANE Select ENSP00000382166.3:p.Lys310AsnfsTer29
ENST00000358309.3:c.1023del ENSP00000351059.3:p.Lys342AsnfsTer29
ENST00000399220.2:c.927del ENSP00000382166.2:p.Lys310AsnfsTer29
ENST00000541347.5:c.927del ENSP00000439140.1:p.Lys310AsnfsTer29
ENST00000542107.5:c.927del ENSP00000444928.1:p.Lys310AsnfsTer29
NM_001171171.1:c.927del NP_001164642.1:p.Lys310AsnfsTer29
NM_001171172.1:c.927del NP_001164643.1:p.Lys310AsnfsTer29
NM_001171174.1:c.1023del NP_001164645.1:p.Lys342AsnfsTer29
NM_001337.3:c.927del NP_001328.1:p.Lys310AsnfsTer29
NM_001337.4:c.927del MANE Select NP_001328.1:p.Lys310AsnfsTer29
NM_001171171.2:c.927del NP_001164642.1:p.Lys310AsnfsTer29
NM_001171172.2:c.927del NP_001164643.1:p.Lys310AsnfsTer29