Canonical Allele Identifier: CA348659164

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873085A>G (hg19) ; chr2:g.136115515A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115515A>G , CM000664.2:g.136115515A>G	GRCh38
NC_000002.11:g.136873085A>G , CM000664.1:g.136873085A>G	GRCh37
NC_000002.10:g.136589555A>G	NCBI36
NG_011587.1:g.7641T>C , LRG_51:g.7641T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.401T>C	ENSP00000512428.1:p.Ile134Thr
ENST00000696137.1:c.368T>C	ENSP00000512429.1:p.Ile123Thr
ENST00000696152.1:c.368T>C	ENSP00000512443.1:p.Ile123Thr
ENST00000696228.1:c.401T>C	ENSP00000512494.1:p.Ile134Thr
ENST00000241393.4:c.413T>C MANE Select	ENSP00000241393.3:p.Ile138Thr
ENST00000241393.3:c.413T>C	ENSP00000241393.3:p.Ile138Thr
ENST00000409817.1:c.425T>C	ENSP00000386884.1:p.Ile142Thr
ENST00000466288.1:n.607T>C
NM_001008540.1:c.425T>C	NP_001008540.1:p.Ile142Thr
NM_003467.2:c.413T>C , LRG_51t1:c.413T>C	NP_003458.1:p.Ile138Thr
NM_001008540.2:c.425T>C	NP_001008540.1:p.Ile142Thr
NM_001348056.1:c.626T>C	NP_001334985.1:p.Ile209Thr
NM_001348059.1:c.512T>C	NP_001334988.1:p.Ile171Thr
NM_001348060.1:c.368T>C	NP_001334989.1:p.Ile123Thr
NM_001348056.2:c.626T>C	NP_001334985.1:p.Ile209Thr
NM_001348059.2:c.512T>C	NP_001334988.1:p.Ile171Thr
NM_001348060.2:c.368T>C	NP_001334989.1:p.Ile123Thr
NM_003467.3:c.413T>C MANE Select	NP_003458.1:p.Ile138Thr