Canonical Allele Identifier: CA2509647815
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255998_34256003del , CM000679.2:g.34255998_34256003del GRCh38
NC_000017.10:g.32583017_32583022del , CM000679.1:g.32583017_32583022del GRCh37
NC_000017.9:g.29607130_29607135del NCBI36
NG_012123.1:g.5722_5727del

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-224_77-219del ENSP00000462156.1:n.77-224_77-219del
ENST00000624362.2:n.714_719del
ENST00000225831.4:c.77-224_77-219del MANE Select ENSP00000225831.4:n.77-224_77-219del
ENST00000580907.5:c.77-224_77-219del ENSP00000462156.1:n.77-224_77-219del
ENST00000624362.1:n.781_786del
NM_002982.3:c.77-224_77-219del NP_002973.1:n.77-224_77-219del
NM_002982.4:c.77-224_77-219del MANE Select NP_002973.1:n.77-224_77-219del