Canonical Allele Identifier: CA348659622

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873169T>C (hg19) ; chr2:g.136115599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115599T>C , CM000664.2:g.136115599T>C	GRCh38
NC_000002.11:g.136873169T>C , CM000664.1:g.136873169T>C	GRCh37
NC_000002.10:g.136589639T>C	NCBI36
NG_011587.1:g.7557A>G , LRG_51:g.7557A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.317A>G	ENSP00000512428.1:p.Lys106Arg
ENST00000696137.1:c.284A>G	ENSP00000512429.1:p.Lys95Arg
ENST00000696152.1:c.284A>G	ENSP00000512443.1:p.Lys95Arg
ENST00000696228.1:c.317A>G	ENSP00000512494.1:p.Lys106Arg
ENST00000241393.4:c.329A>G MANE Select	ENSP00000241393.3:p.Lys110Arg
ENST00000241393.3:c.329A>G	ENSP00000241393.3:p.Lys110Arg
ENST00000409817.1:c.341A>G	ENSP00000386884.1:p.Lys114Arg
ENST00000466288.1:n.523A>G
NM_001008540.1:c.341A>G	NP_001008540.1:p.Lys114Arg
NM_003467.2:c.329A>G , LRG_51t1:c.329A>G	NP_003458.1:p.Lys110Arg
NM_001008540.2:c.341A>G	NP_001008540.1:p.Lys114Arg
NM_001348056.1:c.542A>G	NP_001334985.1:p.Lys181Arg
NM_001348059.1:c.428A>G	NP_001334988.1:p.Lys143Arg
NM_001348060.1:c.284A>G	NP_001334989.1:p.Lys95Arg
NM_001348056.2:c.542A>G	NP_001334985.1:p.Lys181Arg
NM_001348059.2:c.428A>G	NP_001334988.1:p.Lys143Arg
NM_001348060.2:c.284A>G	NP_001334989.1:p.Lys95Arg
NM_003467.3:c.329A>G MANE Select	NP_003458.1:p.Lys110Arg