Canonical Allele Identifier: CA2665159062

Gene: CX3CR1

Linked Data

• gnomAD v4: 3-39265324-T-TGCATTGGGTCCATCATTTTGTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265325_39265347dup , CM000665.2:g.39265325_39265347dup	GRCh38
NC_000003.11:g.39306816_39306838dup , CM000665.1:g.39306816_39306838dup	GRCh37
NC_000003.10:g.39281820_39281842dup	NCBI36
NG_016362.1:g.21389_21411dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.*95_*117dup MANE Select	ENSP00000382166.3:n.*95_*117dup
ENST00000358309.3:c.*95_*117dup	ENSP00000351059.3:n.*95_*117dup
ENST00000399220.2:c.*95_*117dup	ENSP00000382166.2:n.*95_*117dup
ENST00000541347.5:c.*95_*117dup	ENSP00000439140.1:n.*95_*117dup
ENST00000542107.5:c.*95_*117dup	ENSP00000444928.1:n.*95_*117dup
NM_001171171.1:c.*95_*117dup	NP_001164642.1:n.*95_*117dup
NM_001171172.1:c.*95_*117dup	NP_001164643.1:n.*95_*117dup
NM_001171174.1:c.*95_*117dup	NP_001164645.1:n.*95_*117dup
NM_001337.3:c.*95_*117dup	NP_001328.1:n.*95_*117dup
NM_001337.4:c.*95_*117dup MANE Select	NP_001328.1:n.*95_*117dup
NM_001171171.2:c.*95_*117dup	NP_001164642.1:n.*95_*117dup
NM_001171172.2:c.*95_*117dup	NP_001164643.1:n.*95_*117dup