Canonical Allele Identifier: CA1290966093

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115590T= , CM000664.2:g.136115590T=	GRCh38
NC_000002.11:g.136873160T= , CM000664.1:g.136873160T=	GRCh37
NC_000002.10:g.136589630T=	NCBI36
NG_011587.1:g.7566A= , LRG_51:g.7566A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.326A=	ENSP00000512428.1:p.His109=
ENST00000696137.1:c.293A=	ENSP00000512429.1:p.His98=
ENST00000696152.1:c.293A=	ENSP00000512443.1:p.His98=
ENST00000696228.1:c.326A=	ENSP00000512494.1:p.His109=
ENST00000241393.4:c.338A= MANE Select	ENSP00000241393.3:p.His113=
ENST00000241393.3:c.338A=	ENSP00000241393.3:p.His113=
ENST00000409817.1:c.350A=	ENSP00000386884.1:p.His117=
ENST00000466288.1:n.532A=
NM_001008540.1:c.350A=	NP_001008540.1:p.His117=
NM_003467.2:c.338A= , LRG_51t1:c.338A=	NP_003458.1:p.His113=
NM_001008540.2:c.350A=	NP_001008540.1:p.His117=
NM_001348056.1:c.551A=	NP_001334985.1:p.His184=
NM_001348059.1:c.437A=	NP_001334988.1:p.His146=
NM_001348060.1:c.293A=	NP_001334989.1:p.His98=
NM_001348056.2:c.551A=	NP_001334985.1:p.His184=
NM_001348059.2:c.437A=	NP_001334988.1:p.His146=
NM_001348060.2:c.293A=	NP_001334989.1:p.His98=
NM_003467.3:c.338A= MANE Select	NP_003458.1:p.His113=