Canonical Allele Identifier: CA543041124

Gene: CCR5 CCR5AS

Linked Data

• dbSNP Id: rs1261756208
• gnomAD v2: 3-46414638-CTGTCCCCTTCTGGGCTCACTA-C
• gnomAD v3: 3-46373147-CTGTCCCCTTCTGGGCTCACTA-C
• gnomAD v4: 3-46373147-CTGTCCCCTTCTGGGCTCACTA-C
• MyVariant Identifiers: chr3:g.46414639_46414659del (hg19) ; chr3:g.46373148_46373168del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46373150_46373170del , CM000665.2:g.46373150_46373170del	GRCh38
NC_000003.11:g.46414641_46414661del , CM000665.1:g.46414641_46414661del	GRCh37
NC_000003.10:g.46389645_46389665del	NCBI36
NG_012637.1:g.8009_8029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000292303.5:c.248_268del (CCR5) MANE Select	ENSP00000292303.4:p.Val83_Tyr89del
ENST00000292303.4:c.248_268del (CCR5)	ENSP00000292303.4:p.Val83_Tyr89del
ENST00000445772.1:c.248_268del (CCR5)	ENSP00000404881.1:p.Val83_Tyr89del
NM_000579.3:c.248_268del (CCR5)	NP_000570.1:p.Val83_Tyr89del
NM_001100168.1:c.248_268del (CCR5)	NP_001093638.1:p.Val83_Tyr89del
NR_125406.1:n.392-1751_392-1731del (CCR5AS)
NM_000579.4:c.248_268del (CCR5)	NP_000570.1:p.Val83_Tyr89del
NM_001100168.2:c.248_268del (CCR5)	NP_001093638.1:p.Val83_Tyr89del
NM_001394783.1:c.248_268del (CCR5) MANE Select	NP_001381712.1:p.Val83_Tyr89del