Canonical Allele Identifier: CA2256959841
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255980_34255994delinsAGCTCCTCCTTCTCT , CM000679.2:g.34255980_34255994delinsAGCTCCTCCTTCTCT GRCh38
NC_000017.10:g.32582999_32583013delinsAGCTCCTCCTTCTCT , CM000679.1:g.32582999_32583013delinsAGCTCCTCCTTCTCT GRCh37
NC_000017.9:g.29607112_29607126delinsAGCTCCTCCTTCTCT NCBI36
NG_012123.1:g.5704_5718delinsAGCTCCTCCTTCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-242_77-228delinsAGCTCCTCCTTCTCT ENSP00000462156.1:n.77-242_77-228delinsAGCTCCTCCTTCTCT
ENST00000624362.2:n.696_710delinsAGCTCCTCCTTCTCT
ENST00000225831.4:c.77-242_77-228delinsAGCTCCTCCTTCTCT MANE Select ENSP00000225831.4:n.77-242_77-228delinsAGCTCCTCCTTCTCT
ENST00000580907.5:c.77-242_77-228delinsAGCTCCTCCTTCTCT ENSP00000462156.1:n.77-242_77-228delinsAGCTCCTCCTTCTCT
ENST00000624362.1:n.763_777delinsAGCTCCTCCTTCTCT
NM_002982.3:c.77-242_77-228delinsAGCTCCTCCTTCTCT NP_002973.1:n.77-242_77-228delinsAGCTCCTCCTTCTCT
NM_002982.4:c.77-242_77-228delinsAGCTCCTCCTTCTCT MANE Select NP_002973.1:n.77-242_77-228delinsAGCTCCTCCTTCTCT