Canonical Allele Identifier: CA2755917400

Gene: CX3CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39279572_39279716del , CM000665.2:g.39279572_39279716del	GRCh38
NC_000003.11:g.39321063_39321207del , CM000665.1:g.39321063_39321207del	GRCh37
NC_000003.10:g.39296067_39296211del	NCBI36
NG_016362.1:g.7020_7164del

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.-10+238_-10+382del MANE Select	ENSP00000382166.3:n.-10+238_-10+382del
ENST00000358309.3:c.87+1893_87+2037del	ENSP00000351059.3:n.87+1893_87+2037del
ENST00000399220.2:c.-10+238_-10+382del	ENSP00000382166.2:n.-10+238_-10+382del
ENST00000412814.1:c.-10+1327_-10+1471del	ENSP00000408835.1:n.-10+1327_-10+1471del
ENST00000435290.1:c.-10+533_-10+677del	ENSP00000394960.1:n.-10+533_-10+677del
ENST00000541347.5:c.-10+1327_-10+1471del	ENSP00000439140.1:n.-10+1327_-10+1471del
ENST00000542107.5:c.-10+533_-10+677del	ENSP00000444928.1:n.-10+533_-10+677del
NM_001171171.1:c.-10+1327_-10+1471del	NP_001164642.1:n.-10+1327_-10+1471del
NM_001171172.1:c.-10+533_-10+677del	NP_001164643.1:n.-10+533_-10+677del
NM_001171174.1:c.87+1893_87+2037del	NP_001164645.1:n.87+1893_87+2037del
NM_001337.3:c.-10+238_-10+382del	NP_001328.1:n.-10+238_-10+382del
NM_001337.4:c.-10+238_-10+382del MANE Select	NP_001328.1:n.-10+238_-10+382del
NM_001171171.2:c.-10+1327_-10+1471del	NP_001164642.1:n.-10+1327_-10+1471del
NM_001171172.2:c.-10+533_-10+677del	NP_001164643.1:n.-10+533_-10+677del