Canonical Allele Identifier: CA2256960005

Gene: CCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.34256381_34256382delinsCT , CM000679.2:g.34256381_34256382delinsCT	GRCh38
NC_000017.10:g.32583400_32583401delinsCT , CM000679.1:g.32583400_32583401delinsCT	GRCh37
NC_000017.9:g.29607513_29607514delinsCT	NCBI36
NG_012123.1:g.6105_6106delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580907.6:c.*38_*39delinsCT	ENSP00000462156.1:n.*38_*39delinsCT
ENST00000624362.2:n.1097_1098delinsCT
ENST00000225831.4:c.194+42_194+43delinsCT MANE Select	ENSP00000225831.4:n.194+42_194+43delinsCT
ENST00000580907.5:c.*38_*39delinsCT	ENSP00000462156.1:n.*38_*39delinsCT
ENST00000582017.1:n.174_175delinsCT
NM_002982.3:c.194+42_194+43delinsCT	NP_002973.1:n.194+42_194+43delinsCT
NM_002982.4:c.194+42_194+43delinsCT MANE Select	NP_002973.1:n.194+42_194+43delinsCT