Canonical Allele Identifier: CA1047048674

Gene: CX3CR1

Linked Data

• dbSNP Id: rs2040683347
• gnomAD v3: 3-39265539-A-AAATC
• gnomAD v4: 3-39265539-A-AAATC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265542_39265545dup , CM000665.2:g.39265542_39265545dup	GRCh38
NC_000003.11:g.39307033_39307036dup , CM000665.1:g.39307033_39307036dup	GRCh37
NC_000003.10:g.39282037_39282040dup	NCBI36
NG_016362.1:g.21193_21196dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.967_970dup MANE Select	ENSP00000382166.3:p.Phe324Ter
ENST00000358309.3:c.1063_1066dup	ENSP00000351059.3:p.Phe356Ter
ENST00000399220.2:c.967_970dup	ENSP00000382166.2:p.Phe324Ter
ENST00000541347.5:c.967_970dup	ENSP00000439140.1:p.Phe324Ter
ENST00000542107.5:c.967_970dup	ENSP00000444928.1:p.Phe324Ter
NM_001171171.1:c.967_970dup	NP_001164642.1:p.Phe324Ter
NM_001171172.1:c.967_970dup	NP_001164643.1:p.Phe324Ter
NM_001171174.1:c.1063_1066dup	NP_001164645.1:p.Phe356Ter
NM_001337.3:c.967_970dup	NP_001328.1:p.Phe324Ter
NM_001337.4:c.967_970dup MANE Select	NP_001328.1:p.Phe324Ter
NM_001171171.2:c.967_970dup	NP_001164642.1:p.Phe324Ter
NM_001171172.2:c.967_970dup	NP_001164643.1:p.Phe324Ter