Canonical Allele Identifier: CA348659175

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873088G>A (hg19) ; chr2:g.136115518G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115518G>A , CM000664.2:g.136115518G>A	GRCh38
NC_000002.11:g.136873088G>A , CM000664.1:g.136873088G>A	GRCh37
NC_000002.10:g.136589558G>A	NCBI36
NG_011587.1:g.7638C>T , LRG_51:g.7638C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.398C>T	ENSP00000512428.1:p.Ala133Val
ENST00000696137.1:c.365C>T	ENSP00000512429.1:p.Ala122Val
ENST00000696152.1:c.365C>T	ENSP00000512443.1:p.Ala122Val
ENST00000696228.1:c.398C>T	ENSP00000512494.1:p.Ala133Val
ENST00000241393.4:c.410C>T MANE Select	ENSP00000241393.3:p.Ala137Val
ENST00000241393.3:c.410C>T	ENSP00000241393.3:p.Ala137Val
ENST00000409817.1:c.422C>T	ENSP00000386884.1:p.Ala141Val
ENST00000466288.1:n.604C>T
NM_001008540.1:c.422C>T	NP_001008540.1:p.Ala141Val
NM_003467.2:c.410C>T , LRG_51t1:c.410C>T	NP_003458.1:p.Ala137Val
NM_001008540.2:c.422C>T	NP_001008540.1:p.Ala141Val
NM_001348056.1:c.623C>T	NP_001334985.1:p.Ala208Val
NM_001348059.1:c.509C>T	NP_001334988.1:p.Ala170Val
NM_001348060.1:c.365C>T	NP_001334989.1:p.Ala122Val
NM_001348056.2:c.623C>T	NP_001334985.1:p.Ala208Val
NM_001348059.2:c.509C>T	NP_001334988.1:p.Ala170Val
NM_001348060.2:c.365C>T	NP_001334989.1:p.Ala122Val
NM_003467.3:c.410C>T MANE Select	NP_003458.1:p.Ala137Val