Canonical Allele Identifier: CA2576229456
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255420_34255421insAGGG , CM000679.2:g.34255420_34255421insAGGG GRCh38
NC_000017.10:g.32582439_32582440insAGGG , CM000679.1:g.32582439_32582440insAGGG GRCh37
NC_000017.9:g.29606552_29606553insAGGG NCBI36
NG_012123.1:g.5144_5145insAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.71_72insAGGG ENSP00000462156.1:p.Pro25GlyfsTer14
ENST00000624362.2:n.136_137insAGGG
ENST00000225831.4:c.71_72insAGGG MANE Select ENSP00000225831.4:p.Pro25GlyfsTer14
ENST00000580907.5:c.71_72insAGGG ENSP00000462156.1:p.Pro25GlyfsTer14
ENST00000624362.1:n.203_204insAGGG
NM_002982.3:c.71_72insAGGG NP_002973.1:p.Pro25GlyfsTer14
NM_002982.4:c.71_72insAGGG MANE Select NP_002973.1:p.Pro25GlyfsTer14
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