Canonical Allele Identifier: CA2256959845
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255983_34255993delinsTCCTCCTTCTC , CM000679.2:g.34255983_34255993delinsTCCTCCTTCTC GRCh38
NC_000017.10:g.32583002_32583012delinsTCCTCCTTCTC , CM000679.1:g.32583002_32583012delinsTCCTCCTTCTC GRCh37
NC_000017.9:g.29607115_29607125delinsTCCTCCTTCTC NCBI36
NG_012123.1:g.5707_5717delinsTCCTCCTTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-239_77-229delinsTCCTCCTTCTC ENSP00000462156.1:n.77-239_77-229delinsTCCTCCTTCTC
ENST00000624362.2:n.699_709delinsTCCTCCTTCTC
ENST00000225831.4:c.77-239_77-229delinsTCCTCCTTCTC MANE Select ENSP00000225831.4:n.77-239_77-229delinsTCCTCCTTCTC
ENST00000580907.5:c.77-239_77-229delinsTCCTCCTTCTC ENSP00000462156.1:n.77-239_77-229delinsTCCTCCTTCTC
ENST00000624362.1:n.766_776delinsTCCTCCTTCTC
NM_002982.3:c.77-239_77-229delinsTCCTCCTTCTC NP_002973.1:n.77-239_77-229delinsTCCTCCTTCTC
NM_002982.4:c.77-239_77-229delinsTCCTCCTTCTC MANE Select NP_002973.1:n.77-239_77-229delinsTCCTCCTTCTC