Canonical Allele Identifier: CA1290965872

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136114901C= , CM000664.2:g.136114901C=	GRCh38
NC_000002.11:g.136872471C= , CM000664.1:g.136872471C=	GRCh37
NC_000002.10:g.136588941C=	NCBI36
NG_011587.1:g.8255G= , LRG_51:g.8255G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.1015G=	ENSP00000512428.1:p.Glu339=
ENST00000696137.1:c.982G=	ENSP00000512429.1:p.Glu328=
ENST00000696152.1:c.982G=	ENSP00000512443.1:p.Glu328=
ENST00000696228.1:c.1015G=	ENSP00000512494.1:p.Glu339=
ENST00000241393.4:c.1027G= MANE Select	ENSP00000241393.3:p.Glu343=
ENST00000241393.3:c.1027G=	ENSP00000241393.3:p.Glu343=
ENST00000409817.1:c.1039G=	ENSP00000386884.1:p.Glu347=
ENST00000466288.1:n.1221G=
NM_001008540.1:c.1039G=	NP_001008540.1:p.Glu347=
NM_003467.2:c.1027G= , LRG_51t1:c.1027G=	NP_003458.1:p.Glu343=
NM_001008540.2:c.1039G=	NP_001008540.1:p.Glu347=
NM_001348056.1:c.1240G=	NP_001334985.1:p.Glu414=
NM_001348059.1:c.1126G=	NP_001334988.1:p.Glu376=
NM_001348060.1:c.982G=	NP_001334989.1:p.Glu328=
NM_001348056.2:c.1240G=	NP_001334985.1:p.Glu414=
NM_001348059.2:c.1126G=	NP_001334988.1:p.Glu376=
NM_001348060.2:c.982G=	NP_001334989.1:p.Glu328=
NM_003467.3:c.1027G= MANE Select	NP_003458.1:p.Glu343=