Canonical Allele Identifier: CA348659650
Gene: CXCR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.136115610G>T , CM000664.2:g.136115610G>T GRCh38
NC_000002.11:g.136873180G>T , CM000664.1:g.136873180G>T GRCh37
NC_000002.10:g.136589650G>T NCBI36
NG_011587.1:g.7546C>A , LRG_51:g.7546C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696136.1:c.306C>A ENSP00000512428.1:p.Asn102Lys
ENST00000696137.1:c.273C>A ENSP00000512429.1:p.Asn91Lys
ENST00000696152.1:c.273C>A ENSP00000512443.1:p.Asn91Lys
ENST00000696228.1:c.306C>A ENSP00000512494.1:p.Asn102Lys
ENST00000241393.4:c.318C>A MANE Select ENSP00000241393.3:p.Asn106Lys
ENST00000241393.3:c.318C>A ENSP00000241393.3:p.Asn106Lys
ENST00000409817.1:c.330C>A ENSP00000386884.1:p.Asn110Lys
ENST00000466288.1:n.512C>A
NM_001008540.1:c.330C>A NP_001008540.1:p.Asn110Lys
NM_003467.2:c.318C>A , LRG_51t1:c.318C>A NP_003458.1:p.Asn106Lys
NM_001008540.2:c.330C>A NP_001008540.1:p.Asn110Lys
NM_001348056.1:c.531C>A NP_001334985.1:p.Asn177Lys
NM_001348059.1:c.417C>A NP_001334988.1:p.Asn139Lys
NM_001348060.1:c.273C>A NP_001334989.1:p.Asn91Lys
NM_001348056.2:c.531C>A NP_001334985.1:p.Asn177Lys
NM_001348059.2:c.417C>A NP_001334988.1:p.Asn139Lys
NM_001348060.2:c.273C>A NP_001334989.1:p.Asn91Lys
NM_003467.3:c.318C>A MANE Select NP_003458.1:p.Asn106Lys