Canonical Allele Identifier: CA433592580
Gene: CCR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46357619_46357620del , CM000665.2:g.46357619_46357620del GRCh38
NC_000003.11:g.46399110_46399111del , CM000665.1:g.46399110_46399111del GRCh37
NC_000003.10:g.46374114_46374115del NCBI36
NG_021428.1:g.8876_8877del

Transcript Alleles

HGVS Amino-acid change
ENST00000445132.3:c.92_93del MANE Select ENSP00000399285.2:p.Pro31LeufsTer3
ENST00000292301.4:c.92_93del ENSP00000292301.3:p.Pro31LeufsTer3
ENST00000400888.2:c.92_93del ENSP00000383681.2:p.Pro31LeufsTer3
ENST00000421659.1:c.92_93del ENSP00000396736.1:p.Pro31LeufsTer3
ENST00000445132.2:c.92_93del ENSP00000399285.2:p.Pro31LeufsTer3
ENST00000465202.1:n.315-498_315-497del
NM_001123041.2:c.92_93del NP_001116513.2:p.Pro31LeufsTer3
NM_001123396.1:c.92_93del NP_001116868.1:p.Pro31LeufsTer3
XM_011534069.1:c.92_93del XP_011532371.1:p.Pro31LeufsTer3
NM_001123396.2:c.92_93del NP_001116868.1:p.Pro31LeufsTer3
NM_001123396.3:c.92_93del NP_001116868.1:p.Pro31LeufsTer3
NM_001123041.3:c.92_93del NP_001116513.2:p.Pro31LeufsTer3
NM_001123396.4:c.92_93del MANE Select NP_001116868.1:p.Pro31LeufsTer3