Canonical Allele Identifier: CA1290966080

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115524T= , CM000664.2:g.136115524T=	GRCh38
NC_000002.11:g.136873094T= , CM000664.1:g.136873094T=	GRCh37
NC_000002.10:g.136589564T=	NCBI36
NG_011587.1:g.7632A= , LRG_51:g.7632A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.392A=	ENSP00000512428.1:p.Tyr131=
ENST00000696137.1:c.359A=	ENSP00000512429.1:p.Tyr120=
ENST00000696152.1:c.359A=	ENSP00000512443.1:p.Tyr120=
ENST00000696228.1:c.392A=	ENSP00000512494.1:p.Tyr131=
ENST00000241393.4:c.404A= MANE Select	ENSP00000241393.3:p.Tyr135=
ENST00000241393.3:c.404A=	ENSP00000241393.3:p.Tyr135=
ENST00000409817.1:c.416A=	ENSP00000386884.1:p.Tyr139=
ENST00000466288.1:n.598A=
NM_001008540.1:c.416A=	NP_001008540.1:p.Tyr139=
NM_003467.2:c.404A= , LRG_51t1:c.404A=	NP_003458.1:p.Tyr135=
NM_001008540.2:c.416A=	NP_001008540.1:p.Tyr139=
NM_001348056.1:c.617A=	NP_001334985.1:p.Tyr206=
NM_001348059.1:c.503A=	NP_001334988.1:p.Tyr168=
NM_001348060.1:c.359A=	NP_001334989.1:p.Tyr120=
NM_001348056.2:c.617A=	NP_001334985.1:p.Tyr206=
NM_001348059.2:c.503A=	NP_001334988.1:p.Tyr168=
NM_001348060.2:c.359A=	NP_001334989.1:p.Tyr120=
NM_003467.3:c.404A= MANE Select	NP_003458.1:p.Tyr135=