Canonical Allele Identifier: CA352473589

Linked Data

gnomAD v4: 3-46373896-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373896C>T , CM000665.2:g.46373896C>T GRCh38
NC_000003.11:g.46415387C>T , CM000665.1:g.46415387C>T GRCh37
NC_000003.10:g.46390391C>T NCBI36
NG_012637.1:g.8755C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.994C>T (CCR5) MANE Select ENSP00000292303.4:p.Pro332Ser
ENST00000292303.4:c.994C>T (CCR5) ENSP00000292303.4:p.Pro332Ser
ENST00000445772.1:c.994C>T (CCR5) ENSP00000404881.1:p.Pro332Ser
NM_000579.3:c.994C>T (CCR5) NP_000570.1:p.Pro332Ser
NM_001100168.1:c.994C>T (CCR5) NP_001093638.1:p.Pro332Ser
NR_125406.1:n.392-2479G>A (CCR5AS)
NM_000579.4:c.994C>T (CCR5) NP_000570.1:p.Pro332Ser
NM_001100168.2:c.994C>T (CCR5) NP_001093638.1:p.Pro332Ser
NM_001394783.1:c.994C>T (CCR5) MANE Select NP_001381712.1:p.Pro332Ser