Canonical Allele Identifier: CA348659389

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873131T>G (hg19) ; chr2:g.136115561T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115561T>G , CM000664.2:g.136115561T>G	GRCh38
NC_000002.11:g.136873131T>G , CM000664.1:g.136873131T>G	GRCh37
NC_000002.10:g.136589601T>G	NCBI36
NG_011587.1:g.7595A>C , LRG_51:g.7595A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.355A>C	ENSP00000512428.1:p.Ser119Arg
ENST00000696137.1:c.322A>C	ENSP00000512429.1:p.Ser108Arg
ENST00000696152.1:c.322A>C	ENSP00000512443.1:p.Ser108Arg
ENST00000696228.1:c.355A>C	ENSP00000512494.1:p.Ser119Arg
ENST00000241393.4:c.367A>C MANE Select	ENSP00000241393.3:p.Ser123Arg
ENST00000241393.3:c.367A>C	ENSP00000241393.3:p.Ser123Arg
ENST00000409817.1:c.379A>C	ENSP00000386884.1:p.Ser127Arg
ENST00000466288.1:n.561A>C
NM_001008540.1:c.379A>C	NP_001008540.1:p.Ser127Arg
NM_003467.2:c.367A>C , LRG_51t1:c.367A>C	NP_003458.1:p.Ser123Arg
NM_001008540.2:c.379A>C	NP_001008540.1:p.Ser127Arg
NM_001348056.1:c.580A>C	NP_001334985.1:p.Ser194Arg
NM_001348059.1:c.466A>C	NP_001334988.1:p.Ser156Arg
NM_001348060.1:c.322A>C	NP_001334989.1:p.Ser108Arg
NM_001348056.2:c.580A>C	NP_001334985.1:p.Ser194Arg
NM_001348059.2:c.466A>C	NP_001334988.1:p.Ser156Arg
NM_001348060.2:c.322A>C	NP_001334989.1:p.Ser108Arg
NM_003467.3:c.367A>C MANE Select	NP_003458.1:p.Ser123Arg