Canonical Allele Identifier: CA348659188

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873091A>C (hg19) ; chr2:g.136115521A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115521A>C , CM000664.2:g.136115521A>C	GRCh38
NC_000002.11:g.136873091A>C , CM000664.1:g.136873091A>C	GRCh37
NC_000002.10:g.136589561A>C	NCBI36
NG_011587.1:g.7635T>G , LRG_51:g.7635T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.395T>G	ENSP00000512428.1:p.Leu132Arg
ENST00000696137.1:c.362T>G	ENSP00000512429.1:p.Leu121Arg
ENST00000696152.1:c.362T>G	ENSP00000512443.1:p.Leu121Arg
ENST00000696228.1:c.395T>G	ENSP00000512494.1:p.Leu132Arg
ENST00000241393.4:c.407T>G MANE Select	ENSP00000241393.3:p.Leu136Arg
ENST00000241393.3:c.407T>G	ENSP00000241393.3:p.Leu136Arg
ENST00000409817.1:c.419T>G	ENSP00000386884.1:p.Leu140Arg
ENST00000466288.1:n.601T>G
NM_001008540.1:c.419T>G	NP_001008540.1:p.Leu140Arg
NM_003467.2:c.407T>G , LRG_51t1:c.407T>G	NP_003458.1:p.Leu136Arg
NM_001008540.2:c.419T>G	NP_001008540.1:p.Leu140Arg
NM_001348056.1:c.620T>G	NP_001334985.1:p.Leu207Arg
NM_001348059.1:c.506T>G	NP_001334988.1:p.Leu169Arg
NM_001348060.1:c.362T>G	NP_001334989.1:p.Leu121Arg
NM_001348056.2:c.620T>G	NP_001334985.1:p.Leu207Arg
NM_001348059.2:c.506T>G	NP_001334988.1:p.Leu169Arg
NM_001348060.2:c.362T>G	NP_001334989.1:p.Leu121Arg
NM_003467.3:c.407T>G MANE Select	NP_003458.1:p.Leu136Arg