Canonical Allele Identifier: CA1358889100

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39279655G= , CM000665.2:g.39279655G=	GRCh38
NC_000003.11:g.39321146G= , CM000665.1:g.39321146G=	GRCh37
NC_000003.10:g.39296150G=	NCBI36
NG_016362.1:g.7081C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.-10+299C= MANE Select	ENSP00000382166.3:n.-10+299C=
ENST00000358309.3:c.87+1954C=	ENSP00000351059.3:n.87+1954C=
ENST00000399220.2:c.-10+299C=	ENSP00000382166.2:n.-10+299C=
ENST00000412814.1:c.-10+1388C=	ENSP00000408835.1:n.-10+1388C=
ENST00000435290.1:c.-10+594C=	ENSP00000394960.1:n.-10+594C=
ENST00000541347.5:c.-10+1388C=	ENSP00000439140.1:n.-10+1388C=
ENST00000542107.5:c.-10+594C=	ENSP00000444928.1:n.-10+594C=
NM_001171171.1:c.-10+1388C=	NP_001164642.1:n.-10+1388C=
NM_001171172.1:c.-10+594C=	NP_001164643.1:n.-10+594C=
NM_001171174.1:c.87+1954C=	NP_001164645.1:n.87+1954C=
NM_001337.3:c.-10+299C=	NP_001328.1:n.-10+299C=
NM_001337.4:c.-10+299C= MANE Select	NP_001328.1:n.-10+299C=
NM_001171171.2:c.-10+1388C=	NP_001164642.1:n.-10+1388C=
NM_001171172.2:c.-10+594C=	NP_001164643.1:n.-10+594C=