Canonical Allele Identifier: CA348659178

Gene: CXCR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.398C>A	ENSP00000512428.1:p.Ala133Asp
ENST00000696137.1:c.365C>A	ENSP00000512429.1:p.Ala122Asp
ENST00000696152.1:c.365C>A	ENSP00000512443.1:p.Ala122Asp
ENST00000696228.1:c.398C>A	ENSP00000512494.1:p.Ala133Asp
ENST00000241393.4:c.410C>A MANE Select	ENSP00000241393.3:p.Ala137Asp
ENST00000241393.3:c.410C>A	ENSP00000241393.3:p.Ala137Asp
ENST00000409817.1:c.422C>A	ENSP00000386884.1:p.Ala141Asp
ENST00000466288.1:n.604C>A
NM_001008540.1:c.422C>A	NP_001008540.1:p.Ala141Asp
NM_003467.2:c.410C>A , LRG_51t1:c.410C>A	NP_003458.1:p.Ala137Asp
NM_001008540.2:c.422C>A	NP_001008540.1:p.Ala141Asp
NM_001348056.1:c.623C>A	NP_001334985.1:p.Ala208Asp
NM_001348059.1:c.509C>A	NP_001334988.1:p.Ala170Asp
NM_001348060.1:c.365C>A	NP_001334989.1:p.Ala122Asp
NM_001348056.2:c.623C>A	NP_001334985.1:p.Ala208Asp
NM_001348059.2:c.509C>A	NP_001334988.1:p.Ala170Asp
NM_001348060.2:c.365C>A	NP_001334989.1:p.Ala122Asp
NM_003467.3:c.410C>A MANE Select	NP_003458.1:p.Ala137Asp