Canonical Allele Identifier: CA2256959838
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255978_34255992delinsACAGCTCCTCCTTCT , CM000679.2:g.34255978_34255992delinsACAGCTCCTCCTTCT GRCh38
NC_000017.10:g.32582997_32583011delinsACAGCTCCTCCTTCT , CM000679.1:g.32582997_32583011delinsACAGCTCCTCCTTCT GRCh37
NC_000017.9:g.29607110_29607124delinsACAGCTCCTCCTTCT NCBI36
NG_012123.1:g.5702_5716delinsACAGCTCCTCCTTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-244_77-230delinsACAGCTCCTCCTTCT ENSP00000462156.1:n.77-244_77-230delinsACAGCTCCTCCTTCT
ENST00000624362.2:n.694_708delinsACAGCTCCTCCTTCT
ENST00000225831.4:c.77-244_77-230delinsACAGCTCCTCCTTCT MANE Select ENSP00000225831.4:n.77-244_77-230delinsACAGCTCCTCCTTCT
ENST00000580907.5:c.77-244_77-230delinsACAGCTCCTCCTTCT ENSP00000462156.1:n.77-244_77-230delinsACAGCTCCTCCTTCT
ENST00000624362.1:n.761_775delinsACAGCTCCTCCTTCT
NM_002982.3:c.77-244_77-230delinsACAGCTCCTCCTTCT NP_002973.1:n.77-244_77-230delinsACAGCTCCTCCTTCT
NM_002982.4:c.77-244_77-230delinsACAGCTCCTCCTTCT MANE Select NP_002973.1:n.77-244_77-230delinsACAGCTCCTCCTTCT