Canonical Allele Identifier: CA1290965880

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136114925C= , CM000664.2:g.136114925C=	GRCh38
NC_000002.11:g.136872495C= , CM000664.1:g.136872495C=	GRCh37
NC_000002.10:g.136588965C=	NCBI36
NG_011587.1:g.8231G= , LRG_51:g.8231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.991G=	ENSP00000512428.1:p.Gly331=
ENST00000696137.1:c.958G=	ENSP00000512429.1:p.Gly320=
ENST00000696152.1:c.958G=	ENSP00000512443.1:p.Gly320=
ENST00000696228.1:c.991G=	ENSP00000512494.1:p.Gly331=
ENST00000241393.4:c.1003G= MANE Select	ENSP00000241393.3:p.Gly335=
ENST00000241393.3:c.1003G=	ENSP00000241393.3:p.Gly335=
ENST00000409817.1:c.1015G=	ENSP00000386884.1:p.Gly339=
ENST00000466288.1:n.1197G=
NM_001008540.1:c.1015G=	NP_001008540.1:p.Gly339=
NM_003467.2:c.1003G= , LRG_51t1:c.1003G=	NP_003458.1:p.Gly335=
NM_001008540.2:c.1015G=	NP_001008540.1:p.Gly339=
NM_001348056.1:c.1216G=	NP_001334985.1:p.Gly406=
NM_001348059.1:c.1102G=	NP_001334988.1:p.Gly368=
NM_001348060.1:c.958G=	NP_001334989.1:p.Gly320=
NM_001348056.2:c.1216G=	NP_001334985.1:p.Gly406=
NM_001348059.2:c.1102G=	NP_001334988.1:p.Gly368=
NM_001348060.2:c.958G=	NP_001334989.1:p.Gly320=
NM_003467.3:c.1003G= MANE Select	NP_003458.1:p.Gly335=