Canonical Allele Identifier: CA1047054326

Gene: CX3CR1

Linked Data

• gnomAD v3: 3-39279691-G-T
• gnomAD v4: 3-39279691-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39279691G>T , CM000665.2:g.39279691G>T	GRCh38
NC_000003.11:g.39321182G>T , CM000665.1:g.39321182G>T	GRCh37
NC_000003.10:g.39296186G>T	NCBI36
NG_016362.1:g.7045C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.-10+263C>A MANE Select	ENSP00000382166.3:n.-10+263C>A
ENST00000358309.3:c.87+1918C>A	ENSP00000351059.3:n.87+1918C>A
ENST00000399220.2:c.-10+263C>A	ENSP00000382166.2:n.-10+263C>A
ENST00000412814.1:c.-10+1352C>A	ENSP00000408835.1:n.-10+1352C>A
ENST00000435290.1:c.-10+558C>A	ENSP00000394960.1:n.-10+558C>A
ENST00000541347.5:c.-10+1352C>A	ENSP00000439140.1:n.-10+1352C>A
ENST00000542107.5:c.-10+558C>A	ENSP00000444928.1:n.-10+558C>A
NM_001171171.1:c.-10+1352C>A	NP_001164642.1:n.-10+1352C>A
NM_001171172.1:c.-10+558C>A	NP_001164643.1:n.-10+558C>A
NM_001171174.1:c.87+1918C>A	NP_001164645.1:n.87+1918C>A
NM_001337.3:c.-10+263C>A	NP_001328.1:n.-10+263C>A
NM_001337.4:c.-10+263C>A MANE Select	NP_001328.1:n.-10+263C>A
NM_001171171.2:c.-10+1352C>A	NP_001164642.1:n.-10+1352C>A
NM_001171172.2:c.-10+558C>A	NP_001164643.1:n.-10+558C>A