Canonical Allele Identifier: CA1290965882

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136114928G= , CM000664.2:g.136114928G=	GRCh38
NC_000002.11:g.136872498G= , CM000664.1:g.136872498G=	GRCh37
NC_000002.10:g.136588968G=	NCBI36
NG_011587.1:g.8228C= , LRG_51:g.8228C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.988C=	ENSP00000512428.1:p.Arg330=
ENST00000696137.1:c.955C=	ENSP00000512429.1:p.Arg319=
ENST00000696152.1:c.955C=	ENSP00000512443.1:p.Arg319=
ENST00000696228.1:c.988C=	ENSP00000512494.1:p.Arg330=
ENST00000241393.4:c.1000C= MANE Select	ENSP00000241393.3:p.Arg334=
ENST00000241393.3:c.1000C=	ENSP00000241393.3:p.Arg334=
ENST00000409817.1:c.1012C=	ENSP00000386884.1:p.Arg338=
ENST00000466288.1:n.1194C=
NM_001008540.1:c.1012C=	NP_001008540.1:p.Arg338=
NM_003467.2:c.1000C= , LRG_51t1:c.1000C=	NP_003458.1:p.Arg334=
NM_001008540.2:c.1012C=	NP_001008540.1:p.Arg338=
NM_001348056.1:c.1213C=	NP_001334985.1:p.Arg405=
NM_001348059.1:c.1099C=	NP_001334988.1:p.Arg367=
NM_001348060.1:c.955C=	NP_001334989.1:p.Arg319=
NM_001348056.2:c.1213C=	NP_001334985.1:p.Arg405=
NM_001348059.2:c.1099C=	NP_001334988.1:p.Arg367=
NM_001348060.2:c.955C=	NP_001334989.1:p.Arg319=
NM_003467.3:c.1000C= MANE Select	NP_003458.1:p.Arg334=