Canonical Allele Identifier: CA352200437

Gene: CX3CR1

Linked Data

• MyVariant Identifiers: chr3:g.39307200C>A (hg19) ; chr3:g.39265709C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265709C>A , CM000665.2:g.39265709C>A	GRCh38
NC_000003.11:g.39307200C>A , CM000665.1:g.39307200C>A	GRCh37
NC_000003.10:g.39282204C>A	NCBI36
NG_016362.1:g.21027G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.801G>T MANE Select	ENSP00000382166.3:p.Met267Ile
ENST00000358309.3:c.897G>T	ENSP00000351059.3:p.Met299Ile
ENST00000399220.2:c.801G>T	ENSP00000382166.2:p.Met267Ile
ENST00000541347.5:c.801G>T	ENSP00000439140.1:p.Met267Ile
ENST00000542107.5:c.801G>T	ENSP00000444928.1:p.Met267Ile
NM_001171171.1:c.801G>T	NP_001164642.1:p.Met267Ile
NM_001171172.1:c.801G>T	NP_001164643.1:p.Met267Ile
NM_001171174.1:c.897G>T	NP_001164645.1:p.Met299Ile
NM_001337.3:c.801G>T	NP_001328.1:p.Met267Ile
NM_001337.4:c.801G>T MANE Select	NP_001328.1:p.Met267Ile
NM_001171171.2:c.801G>T	NP_001164642.1:p.Met267Ile
NM_001171172.2:c.801G>T	NP_001164643.1:p.Met267Ile