Canonical Allele Identifier: CA2665436443

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373415del , CM000665.2:g.46373415del GRCh38
NC_000003.11:g.46414906del , CM000665.1:g.46414906del GRCh37
NC_000003.10:g.46389910del NCBI36
NG_012637.1:g.8274del

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.513del (CCR5) MANE Select ENSP00000292303.4:p.Glu172LysfsTer25
ENST00000292303.4:c.513del (CCR5) ENSP00000292303.4:p.Glu172LysfsTer25
ENST00000445772.1:c.513del (CCR5) ENSP00000404881.1:p.Glu172LysfsTer25
NM_000579.3:c.513del (CCR5) NP_000570.1:p.Glu172LysfsTer25
NM_001100168.1:c.513del (CCR5) NP_001093638.1:p.Glu172LysfsTer25
NR_125406.1:n.392-1994del (CCR5AS)
NM_000579.4:c.513del (CCR5) NP_000570.1:p.Glu172LysfsTer25
NM_001100168.2:c.513del (CCR5) NP_001093638.1:p.Glu172LysfsTer25
NM_001394783.1:c.513del (CCR5) MANE Select NP_001381712.1:p.Glu172LysfsTer25