Canonical Allele Identifier: CA429206657

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873102C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115532C>T , CM000664.2:g.136115532C>T	GRCh38
NC_000002.11:g.136873102C>T , CM000664.1:g.136873102C>T	GRCh37
NC_000002.10:g.136589572C>T	NCBI36
NG_011587.1:g.7624G>A , LRG_51:g.7624G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.384G>A	ENSP00000512428.1:p.Leu128=
ENST00000696137.1:c.351G>A	ENSP00000512429.1:p.Leu117=
ENST00000696152.1:c.351G>A	ENSP00000512443.1:p.Leu117=
ENST00000696228.1:c.384G>A	ENSP00000512494.1:p.Leu128=
ENST00000241393.4:c.396G>A MANE Select	ENSP00000241393.3:p.Leu132=
ENST00000241393.3:c.396G>A	ENSP00000241393.3:p.Leu132=
ENST00000409817.1:c.408G>A	ENSP00000386884.1:p.Leu136=
ENST00000466288.1:n.590G>A
NM_001008540.1:c.408G>A	NP_001008540.1:p.Leu136=
NM_003467.2:c.396G>A , LRG_51t1:c.396G>A	NP_003458.1:p.Leu132=
NM_001008540.2:c.408G>A	NP_001008540.1:p.Leu136=
NM_001348056.1:c.609G>A	NP_001334985.1:p.Leu203=
NM_001348059.1:c.495G>A	NP_001334988.1:p.Leu165=
NM_001348060.1:c.351G>A	NP_001334989.1:p.Leu117=
NM_001348056.2:c.609G>A	NP_001334985.1:p.Leu203=
NM_001348059.2:c.495G>A	NP_001334988.1:p.Leu165=
NM_001348060.2:c.351G>A	NP_001334989.1:p.Leu117=
NM_003467.3:c.396G>A MANE Select	NP_003458.1:p.Leu132=