Canonical Allele Identifier: CA352201331

Gene: CX3CR1

Linked Data

• gnomAD v4: 3-39265824-G-A
• MyVariant Identifiers: chr3:g.39307315G>A (hg19) ; chr3:g.39265824G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265824G>A , CM000665.2:g.39265824G>A	GRCh38
NC_000003.11:g.39307315G>A , CM000665.1:g.39307315G>A	GRCh37
NC_000003.10:g.39282319G>A	NCBI36
NG_016362.1:g.20912C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.686C>T MANE Select	ENSP00000382166.3:p.Ala229Val
ENST00000358309.3:c.782C>T	ENSP00000351059.3:p.Ala261Val
ENST00000399220.2:c.686C>T	ENSP00000382166.2:p.Ala229Val
ENST00000541347.5:c.686C>T	ENSP00000439140.1:p.Ala229Val
ENST00000542107.5:c.686C>T	ENSP00000444928.1:p.Ala229Val
NM_001171171.1:c.686C>T	NP_001164642.1:p.Ala229Val
NM_001171172.1:c.686C>T	NP_001164643.1:p.Ala229Val
NM_001171174.1:c.782C>T	NP_001164645.1:p.Ala261Val
NM_001337.3:c.686C>T	NP_001328.1:p.Ala229Val
NM_001337.4:c.686C>T MANE Select	NP_001328.1:p.Ala229Val
NM_001171171.2:c.686C>T	NP_001164642.1:p.Ala229Val
NM_001171172.2:c.686C>T	NP_001164643.1:p.Ala229Val