Canonical Allele Identifier: CA348659322

Gene: CXCR4

Linked Data

• gnomAD v4: 2-136115548-A-G
• MyVariant Identifiers: chr2:g.136873118A>G (hg19) ; chr2:g.136115548A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115548A>G , CM000664.2:g.136115548A>G	GRCh38
NC_000002.11:g.136873118A>G , CM000664.1:g.136873118A>G	GRCh37
NC_000002.10:g.136589588A>G	NCBI36
NG_011587.1:g.7608T>C , LRG_51:g.7608T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.368T>C	ENSP00000512428.1:p.Leu123Pro
ENST00000696137.1:c.335T>C	ENSP00000512429.1:p.Leu112Pro
ENST00000696152.1:c.335T>C	ENSP00000512443.1:p.Leu112Pro
ENST00000696228.1:c.368T>C	ENSP00000512494.1:p.Leu123Pro
ENST00000241393.4:c.380T>C MANE Select	ENSP00000241393.3:p.Leu127Pro
ENST00000241393.3:c.380T>C	ENSP00000241393.3:p.Leu127Pro
ENST00000409817.1:c.392T>C	ENSP00000386884.1:p.Leu131Pro
ENST00000466288.1:n.574T>C
NM_001008540.1:c.392T>C	NP_001008540.1:p.Leu131Pro
NM_003467.2:c.380T>C , LRG_51t1:c.380T>C	NP_003458.1:p.Leu127Pro
NM_001008540.2:c.392T>C	NP_001008540.1:p.Leu131Pro
NM_001348056.1:c.593T>C	NP_001334985.1:p.Leu198Pro
NM_001348059.1:c.479T>C	NP_001334988.1:p.Leu160Pro
NM_001348060.1:c.335T>C	NP_001334989.1:p.Leu112Pro
NM_001348056.2:c.593T>C	NP_001334985.1:p.Leu198Pro
NM_001348059.2:c.479T>C	NP_001334988.1:p.Leu160Pro
NM_001348060.2:c.335T>C	NP_001334989.1:p.Leu112Pro
NM_003467.3:c.380T>C MANE Select	NP_003458.1:p.Leu127Pro