Canonical Allele Identifier: CA348659475

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873146C>G (hg19) ; chr2:g.136115576C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115576C>G , CM000664.2:g.136115576C>G	GRCh38
NC_000002.11:g.136873146C>G , CM000664.1:g.136873146C>G	GRCh37
NC_000002.10:g.136589616C>G	NCBI36
NG_011587.1:g.7580G>C , LRG_51:g.7580G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.340G>C	ENSP00000512428.1:p.Val114Leu
ENST00000696137.1:c.307G>C	ENSP00000512429.1:p.Val103Leu
ENST00000696152.1:c.307G>C	ENSP00000512443.1:p.Val103Leu
ENST00000696228.1:c.340G>C	ENSP00000512494.1:p.Val114Leu
ENST00000241393.4:c.352G>C MANE Select	ENSP00000241393.3:p.Val118Leu
ENST00000241393.3:c.352G>C	ENSP00000241393.3:p.Val118Leu
ENST00000409817.1:c.364G>C	ENSP00000386884.1:p.Val122Leu
ENST00000466288.1:n.546G>C
NM_001008540.1:c.364G>C	NP_001008540.1:p.Val122Leu
NM_003467.2:c.352G>C , LRG_51t1:c.352G>C	NP_003458.1:p.Val118Leu
NM_001008540.2:c.364G>C	NP_001008540.1:p.Val122Leu
NM_001348056.1:c.565G>C	NP_001334985.1:p.Val189Leu
NM_001348059.1:c.451G>C	NP_001334988.1:p.Val151Leu
NM_001348060.1:c.307G>C	NP_001334989.1:p.Val103Leu
NM_001348056.2:c.565G>C	NP_001334985.1:p.Val189Leu
NM_001348059.2:c.451G>C	NP_001334988.1:p.Val151Leu
NM_001348060.2:c.307G>C	NP_001334989.1:p.Val103Leu
NM_003467.3:c.352G>C MANE Select	NP_003458.1:p.Val118Leu