Canonical Allele Identifier: CA348659197
Gene: CXCR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.136115523G>T , CM000664.2:g.136115523G>T GRCh38
NC_000002.11:g.136873093G>T , CM000664.1:g.136873093G>T GRCh37
NC_000002.10:g.136589563G>T NCBI36
NG_011587.1:g.7633C>A , LRG_51:g.7633C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696136.1:c.393C>A ENSP00000512428.1:p.Tyr131Ter
ENST00000696137.1:c.360C>A ENSP00000512429.1:p.Tyr120Ter
ENST00000696152.1:c.360C>A ENSP00000512443.1:p.Tyr120Ter
ENST00000696228.1:c.393C>A ENSP00000512494.1:p.Tyr131Ter
ENST00000241393.4:c.405C>A MANE Select ENSP00000241393.3:p.Tyr135Ter
ENST00000241393.3:c.405C>A ENSP00000241393.3:p.Tyr135Ter
ENST00000409817.1:c.417C>A ENSP00000386884.1:p.Tyr139Ter
ENST00000466288.1:n.599C>A
NM_001008540.1:c.417C>A NP_001008540.1:p.Tyr139Ter
NM_003467.2:c.405C>A , LRG_51t1:c.405C>A NP_003458.1:p.Tyr135Ter
NM_001008540.2:c.417C>A NP_001008540.1:p.Tyr139Ter
NM_001348056.1:c.618C>A NP_001334985.1:p.Tyr206Ter
NM_001348059.1:c.504C>A NP_001334988.1:p.Tyr168Ter
NM_001348060.1:c.360C>A NP_001334989.1:p.Tyr120Ter
NM_001348056.2:c.618C>A NP_001334985.1:p.Tyr206Ter
NM_001348059.2:c.504C>A NP_001334988.1:p.Tyr168Ter
NM_001348060.2:c.360C>A NP_001334989.1:p.Tyr120Ter
NM_003467.3:c.405C>A MANE Select NP_003458.1:p.Tyr135Ter