Canonical Allele Identifier: CA2580063827
Gene: CXCR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.136115200del , CM000664.2:g.136115200del GRCh38
NC_000002.11:g.136872770del , CM000664.1:g.136872770del GRCh37
NC_000002.10:g.136589240del NCBI36
NG_011587.1:g.7956del , LRG_51:g.7956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696136.1:c.716del ENSP00000512428.1:p.Ile239ThrfsTer?
ENST00000696137.1:c.683del ENSP00000512429.1:p.Ile228ThrfsTer?
ENST00000696152.1:c.683del ENSP00000512443.1:p.Ile228ThrfsTer?
ENST00000696228.1:c.716del ENSP00000512494.1:p.Ile239ThrfsTer?
ENST00000241393.4:c.728del MANE Select ENSP00000241393.3:p.Ile243ThrfsTer?
ENST00000241393.3:c.728del ENSP00000241393.3:p.Ile243ThrfsTer?
ENST00000409817.1:c.740del ENSP00000386884.1:p.Ile247ThrfsTer?
ENST00000466288.1:n.922del
NM_001008540.1:c.740del NP_001008540.1:p.Ile247ThrfsTer?
NM_003467.2:c.728del , LRG_51t1:c.728del NP_003458.1:p.Ile243ThrfsTer?
NM_001008540.2:c.740del NP_001008540.1:p.Ile247ThrfsTer?
NM_001348056.1:c.941del NP_001334985.1:p.Ile314ThrfsTer?
NM_001348059.1:c.827del NP_001334988.1:p.Ile276ThrfsTer?
NM_001348060.1:c.683del NP_001334989.1:p.Ile228ThrfsTer?
NM_001348056.2:c.941del NP_001334985.1:p.Ile314ThrfsTer?
NM_001348059.2:c.827del NP_001334988.1:p.Ile276ThrfsTer?
NM_001348060.2:c.683del NP_001334989.1:p.Ile228ThrfsTer?
NM_003467.3:c.728del MANE Select NP_003458.1:p.Ile243ThrfsTer?