Canonical Allele Identifier: CA1290966092

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115588C= , CM000664.2:g.136115588C=	GRCh38
NC_000002.11:g.136873158C= , CM000664.1:g.136873158C=	GRCh37
NC_000002.10:g.136589628C=	NCBI36
NG_011587.1:g.7568G= , LRG_51:g.7568G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.328G=	ENSP00000512428.1:p.Val110=
ENST00000696137.1:c.295G=	ENSP00000512429.1:p.Val99=
ENST00000696152.1:c.295G=	ENSP00000512443.1:p.Val99=
ENST00000696228.1:c.328G=	ENSP00000512494.1:p.Val110=
ENST00000241393.4:c.340G= MANE Select	ENSP00000241393.3:p.Val114=
ENST00000241393.3:c.340G=	ENSP00000241393.3:p.Val114=
ENST00000409817.1:c.352G=	ENSP00000386884.1:p.Val118=
ENST00000466288.1:n.534G=
NM_001008540.1:c.352G=	NP_001008540.1:p.Val118=
NM_003467.2:c.340G= , LRG_51t1:c.340G=	NP_003458.1:p.Val114=
NM_001008540.2:c.352G=	NP_001008540.1:p.Val118=
NM_001348056.1:c.553G=	NP_001334985.1:p.Val185=
NM_001348059.1:c.439G=	NP_001334988.1:p.Val147=
NM_001348060.1:c.295G=	NP_001334989.1:p.Val99=
NM_001348056.2:c.553G=	NP_001334985.1:p.Val185=
NM_001348059.2:c.439G=	NP_001334988.1:p.Val147=
NM_001348060.2:c.295G=	NP_001334989.1:p.Val99=
NM_003467.3:c.340G= MANE Select	NP_003458.1:p.Val114=