Canonical Allele Identifier: CA2326882

Gene: CX3CR1

Linked Data

• dbSNP Id: rs766297236
• ExAC: 3:39307092 G / GT
• gnomAD v2: 3-39307092-G-GT
• MyVariant Identifiers: chr3:g.39307092_39307093insT (hg19) ; chr3:g.39265601_39265602insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265602dup , CM000665.2:g.39265602dup	GRCh38
NC_000003.11:g.39307093dup , CM000665.1:g.39307093dup	GRCh37
NC_000003.10:g.39282097dup	NCBI36
NG_016362.1:g.21134dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.908dup MANE Select	ENSP00000382166.3:p.Tyr303Ter
ENST00000358309.3:c.1004dup	ENSP00000351059.3:p.Tyr335Ter
ENST00000399220.2:c.908dup	ENSP00000382166.2:p.Tyr303Ter
ENST00000541347.5:c.908dup	ENSP00000439140.1:p.Tyr303Ter
ENST00000542107.5:c.908dup	ENSP00000444928.1:p.Tyr303Ter
NM_001171171.1:c.908dup	NP_001164642.1:p.Tyr303Ter
NM_001171172.1:c.908dup	NP_001164643.1:p.Tyr303Ter
NM_001171174.1:c.1004dup	NP_001164645.1:p.Tyr335Ter
NM_001337.3:c.908dup	NP_001328.1:p.Tyr303Ter
NM_001337.4:c.908dup MANE Select	NP_001328.1:p.Tyr303Ter
NM_001171171.2:c.908dup	NP_001164642.1:p.Tyr303Ter
NM_001171172.2:c.908dup	NP_001164643.1:p.Tyr303Ter