Canonical Allele Identifier: CA906945576

Gene: CX3CR1

Linked Data

• dbSNP Id: rs1358205953
• gnomAD v3: 3-39265849-AG-A
• gnomAD v4: 3-39265849-AG-A
• MyVariant Identifiers: chr3:g.39307341del (hg19) ; chr3:g.39265850del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265851del , CM000665.2:g.39265851del	GRCh38
NC_000003.11:g.39307342del , CM000665.1:g.39307342del	GRCh37
NC_000003.10:g.39282346del	NCBI36
NG_016362.1:g.20886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.660del MANE Select	ENSP00000382166.3:p.Cys221AlafsTer12
ENST00000358309.3:c.756del	ENSP00000351059.3:p.Cys253AlafsTer12
ENST00000399220.2:c.660del	ENSP00000382166.2:p.Cys221AlafsTer12
ENST00000541347.5:c.660del	ENSP00000439140.1:p.Cys221AlafsTer12
ENST00000542107.5:c.660del	ENSP00000444928.1:p.Cys221AlafsTer12
NM_001171171.1:c.660del	NP_001164642.1:p.Cys221AlafsTer12
NM_001171172.1:c.660del	NP_001164643.1:p.Cys221AlafsTer12
NM_001171174.1:c.756del	NP_001164645.1:p.Cys253AlafsTer12
NM_001337.3:c.660del	NP_001328.1:p.Cys221AlafsTer12
NM_001337.4:c.660del MANE Select	NP_001328.1:p.Cys221AlafsTer12
NM_001171171.2:c.660del	NP_001164642.1:p.Cys221AlafsTer12
NM_001171172.2:c.660del	NP_001164643.1:p.Cys221AlafsTer12