Canonical Allele Identifier: CA348659520

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873154A>G (hg19) ; chr2:g.136115584A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115584A>G , CM000664.2:g.136115584A>G	GRCh38
NC_000002.11:g.136873154A>G , CM000664.1:g.136873154A>G	GRCh37
NC_000002.10:g.136589624A>G	NCBI36
NG_011587.1:g.7572T>C , LRG_51:g.7572T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.332T>C	ENSP00000512428.1:p.Ile111Thr
ENST00000696137.1:c.299T>C	ENSP00000512429.1:p.Ile100Thr
ENST00000696152.1:c.299T>C	ENSP00000512443.1:p.Ile100Thr
ENST00000696228.1:c.332T>C	ENSP00000512494.1:p.Ile111Thr
ENST00000241393.4:c.344T>C MANE Select	ENSP00000241393.3:p.Ile115Thr
ENST00000241393.3:c.344T>C	ENSP00000241393.3:p.Ile115Thr
ENST00000409817.1:c.356T>C	ENSP00000386884.1:p.Ile119Thr
ENST00000466288.1:n.538T>C
NM_001008540.1:c.356T>C	NP_001008540.1:p.Ile119Thr
NM_003467.2:c.344T>C , LRG_51t1:c.344T>C	NP_003458.1:p.Ile115Thr
NM_001008540.2:c.356T>C	NP_001008540.1:p.Ile119Thr
NM_001348056.1:c.557T>C	NP_001334985.1:p.Ile186Thr
NM_001348059.1:c.443T>C	NP_001334988.1:p.Ile148Thr
NM_001348060.1:c.299T>C	NP_001334989.1:p.Ile100Thr
NM_001348056.2:c.557T>C	NP_001334985.1:p.Ile186Thr
NM_001348059.2:c.443T>C	NP_001334988.1:p.Ile148Thr
NM_001348060.2:c.299T>C	NP_001334989.1:p.Ile100Thr
NM_003467.3:c.344T>C MANE Select	NP_003458.1:p.Ile115Thr