Canonical Allele Identifier: CA1358882856

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265795_39265798delinsCGAT , CM000665.2:g.39265795_39265798delinsCGAT	GRCh38
NC_000003.11:g.39307286_39307289delinsCGAT , CM000665.1:g.39307286_39307289delinsCGAT	GRCh37
NC_000003.10:g.39282290_39282293delinsCGAT	NCBI36
NG_016362.1:g.20938_20941delinsATCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.712_715delinsATCG MANE Select	ENSP00000382166.3:p.Ile238=
ENST00000358309.3:c.808_811delinsATCG	ENSP00000351059.3:p.Ile270=
ENST00000399220.2:c.712_715delinsATCG	ENSP00000382166.2:p.Ile238=
ENST00000541347.5:c.712_715delinsATCG	ENSP00000439140.1:p.Ile238=
ENST00000542107.5:c.712_715delinsATCG	ENSP00000444928.1:p.Ile238=
NM_001171171.1:c.712_715delinsATCG	NP_001164642.1:p.Ile238=
NM_001171172.1:c.712_715delinsATCG	NP_001164643.1:p.Ile238=
NM_001171174.1:c.808_811delinsATCG	NP_001164645.1:p.Ile270=
NM_001337.3:c.712_715delinsATCG	NP_001328.1:p.Ile238=
NM_001337.4:c.712_715delinsATCG MANE Select	NP_001328.1:p.Ile238=
NM_001171171.2:c.712_715delinsATCG	NP_001164642.1:p.Ile238=
NM_001171172.2:c.712_715delinsATCG	NP_001164643.1:p.Ile238=