Canonical Allele Identifier: CA543041121

Linked Data

dbSNP Id: rs1406354200

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46372901del , CM000665.2:g.46372901del GRCh38
NC_000003.11:g.46414392del , CM000665.1:g.46414392del GRCh37
NC_000003.10:g.46389396del NCBI36
NG_012637.1:g.7760del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.-2del (CCR5) MANE Select ENSP00000292303.4:n.-2del
ENST00000292303.4:c.-2del (CCR5) ENSP00000292303.4:n.-2del
ENST00000445772.1:c.-2del (CCR5) ENSP00000404881.1:n.-2del
NM_000579.3:c.-2del (CCR5) NP_000570.1:n.-2del
NM_001100168.1:c.-2del (CCR5) NP_001093638.1:n.-2del
NR_125406.1:n.392-1483del (CCR5AS)
NM_000579.4:c.-2del (CCR5) NP_000570.1:n.-2del
NM_001100168.2:c.-2del (CCR5) NP_001093638.1:n.-2del
NM_001394783.1:c.-2del (CCR5) MANE Select NP_001381712.1:n.-2del