Canonical Allele Identifier: CA2354705

Linked Data

dbSNP Id: rs774845977
COSMIC: COSM446586

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373588_46373590del , CM000665.2:g.46373588_46373590del GRCh38
NC_000003.11:g.46415079_46415081del , CM000665.1:g.46415079_46415081del GRCh37
NC_000003.10:g.46390083_46390085del NCBI36
NG_012637.1:g.8447_8449del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.686_688del (CCR5) MANE Select ENSP00000292303.4:p.Lys229del
ENST00000292303.4:c.686_688del (CCR5) ENSP00000292303.4:p.Lys229del
ENST00000445772.1:c.686_688del (CCR5) ENSP00000404881.1:p.Lys229del
NM_000579.3:c.686_688del (CCR5) NP_000570.1:p.Lys229del
NM_001100168.1:c.686_688del (CCR5) NP_001093638.1:p.Lys229del
NR_125406.1:n.392-2167_392-2165del (CCR5AS)
NM_000579.4:c.686_688del (CCR5) NP_000570.1:p.Lys229del
NM_001100168.2:c.686_688del (CCR5) NP_001093638.1:p.Lys229del
NM_001394783.1:c.686_688del (CCR5) MANE Select NP_001381712.1:p.Lys229del