Canonical Allele Identifier: CA1358889124

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39279706C= , CM000665.2:g.39279706C=	GRCh38
NC_000003.11:g.39321197C= , CM000665.1:g.39321197C=	GRCh37
NC_000003.10:g.39296201C=	NCBI36
NG_016362.1:g.7030G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.-10+248G= MANE Select	ENSP00000382166.3:n.-10+248G=
ENST00000358309.3:c.87+1903G=	ENSP00000351059.3:n.87+1903G=
ENST00000399220.2:c.-10+248G=	ENSP00000382166.2:n.-10+248G=
ENST00000412814.1:c.-10+1337G=	ENSP00000408835.1:n.-10+1337G=
ENST00000435290.1:c.-10+543G=	ENSP00000394960.1:n.-10+543G=
ENST00000541347.5:c.-10+1337G=	ENSP00000439140.1:n.-10+1337G=
ENST00000542107.5:c.-10+543G=	ENSP00000444928.1:n.-10+543G=
NM_001171171.1:c.-10+1337G=	NP_001164642.1:n.-10+1337G=
NM_001171172.1:c.-10+543G=	NP_001164643.1:n.-10+543G=
NM_001171174.1:c.87+1903G=	NP_001164645.1:n.87+1903G=
NM_001337.3:c.-10+248G=	NP_001328.1:n.-10+248G=
NM_001337.4:c.-10+248G= MANE Select	NP_001328.1:n.-10+248G=
NM_001171171.2:c.-10+1337G=	NP_001164642.1:n.-10+1337G=
NM_001171172.2:c.-10+543G=	NP_001164643.1:n.-10+543G=