Canonical Allele Identifier: CA348659643

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873178A>C (hg19) ; chr2:g.136115608A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115608A>C , CM000664.2:g.136115608A>C	GRCh38
NC_000002.11:g.136873178A>C , CM000664.1:g.136873178A>C	GRCh37
NC_000002.10:g.136589648A>C	NCBI36
NG_011587.1:g.7548T>G , LRG_51:g.7548T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.308T>G	ENSP00000512428.1:p.Phe103Cys
ENST00000696137.1:c.275T>G	ENSP00000512429.1:p.Phe92Cys
ENST00000696152.1:c.275T>G	ENSP00000512443.1:p.Phe92Cys
ENST00000696228.1:c.308T>G	ENSP00000512494.1:p.Phe103Cys
ENST00000241393.4:c.320T>G MANE Select	ENSP00000241393.3:p.Phe107Cys
ENST00000241393.3:c.320T>G	ENSP00000241393.3:p.Phe107Cys
ENST00000409817.1:c.332T>G	ENSP00000386884.1:p.Phe111Cys
ENST00000466288.1:n.514T>G
NM_001008540.1:c.332T>G	NP_001008540.1:p.Phe111Cys
NM_003467.2:c.320T>G , LRG_51t1:c.320T>G	NP_003458.1:p.Phe107Cys
NM_001008540.2:c.332T>G	NP_001008540.1:p.Phe111Cys
NM_001348056.1:c.533T>G	NP_001334985.1:p.Phe178Cys
NM_001348059.1:c.419T>G	NP_001334988.1:p.Phe140Cys
NM_001348060.1:c.275T>G	NP_001334989.1:p.Phe92Cys
NM_001348056.2:c.533T>G	NP_001334985.1:p.Phe178Cys
NM_001348059.2:c.419T>G	NP_001334988.1:p.Phe140Cys
NM_001348060.2:c.275T>G	NP_001334989.1:p.Phe92Cys
NM_003467.3:c.320T>G MANE Select	NP_003458.1:p.Phe107Cys