Canonical Allele Identifier: CA1362082441

Linked Data

dbSNP Id: rs1701688813

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373114dup , CM000665.2:g.46373114dup GRCh38
NC_000003.11:g.46414605dup , CM000665.1:g.46414605dup GRCh37
NC_000003.10:g.46389609dup NCBI36
NG_012637.1:g.7973dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.212dup (CCR5) MANE Select ENSP00000292303.4:p.Asn71LysfsTer6
ENST00000292303.4:c.212dup (CCR5) ENSP00000292303.4:p.Asn71LysfsTer6
ENST00000445772.1:c.212dup (CCR5) ENSP00000404881.1:p.Asn71LysfsTer6
NM_000579.3:c.212dup (CCR5) NP_000570.1:p.Asn71LysfsTer6
NM_001100168.1:c.212dup (CCR5) NP_001093638.1:p.Asn71LysfsTer6
NR_125406.1:n.392-1696dup (CCR5AS)
NM_000579.4:c.212dup (CCR5) NP_000570.1:p.Asn71LysfsTer6
NM_001100168.2:c.212dup (CCR5) NP_001093638.1:p.Asn71LysfsTer6
NM_001394783.1:c.212dup (CCR5) MANE Select NP_001381712.1:p.Asn71LysfsTer6