Canonical Allele Identifier: CA645539223
Gene: CXCR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.136114965dup , CM000664.2:g.136114965dup GRCh38
NC_000002.11:g.136872535dup , CM000664.1:g.136872535dup GRCh37
NC_000002.10:g.136589005dup NCBI36
NG_011587.1:g.8191dup , LRG_51:g.8191dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696136.1:c.951dup ENSP00000512428.1:p.Arg318GlnfsTer22
ENST00000696137.1:c.918dup ENSP00000512429.1:p.Arg307GlnfsTer22
ENST00000696152.1:c.918dup ENSP00000512443.1:p.Arg307GlnfsTer22
ENST00000696228.1:c.951dup ENSP00000512494.1:p.Arg318GlnfsTer22
ENST00000241393.4:c.963dup MANE Select ENSP00000241393.3:p.Arg322GlnfsTer22
ENST00000241393.3:c.963dup ENSP00000241393.3:p.Arg322GlnfsTer22
ENST00000409817.1:c.975dup ENSP00000386884.1:p.Arg326GlnfsTer22
ENST00000466288.1:n.1157dup
NM_001008540.1:c.975dup NP_001008540.1:p.Arg326GlnfsTer22
NM_003467.2:c.963dup , LRG_51t1:c.963dup NP_003458.1:p.Arg322GlnfsTer22
NM_001008540.2:c.975dup NP_001008540.1:p.Arg326GlnfsTer22
NM_001348056.1:c.1176dup NP_001334985.1:p.Arg393GlnfsTer22
NM_001348059.1:c.1062dup NP_001334988.1:p.Arg355GlnfsTer22
NM_001348060.1:c.918dup NP_001334989.1:p.Arg307GlnfsTer22
NM_001348056.2:c.1176dup NP_001334985.1:p.Arg393GlnfsTer22
NM_001348059.2:c.1062dup NP_001334988.1:p.Arg355GlnfsTer22
NM_001348060.2:c.918dup NP_001334989.1:p.Arg307GlnfsTer22
NM_003467.3:c.963dup MANE Select NP_003458.1:p.Arg322GlnfsTer22