Canonical Allele Identifier: CA348659459

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873143T>A (hg19) ; chr2:g.136115573T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115573T>A , CM000664.2:g.136115573T>A	GRCh38
NC_000002.11:g.136873143T>A , CM000664.1:g.136873143T>A	GRCh37
NC_000002.10:g.136589613T>A	NCBI36
NG_011587.1:g.7583A>T , LRG_51:g.7583A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.343A>T	ENSP00000512428.1:p.Asn115Tyr
ENST00000696137.1:c.310A>T	ENSP00000512429.1:p.Asn104Tyr
ENST00000696152.1:c.310A>T	ENSP00000512443.1:p.Asn104Tyr
ENST00000696228.1:c.343A>T	ENSP00000512494.1:p.Asn115Tyr
ENST00000241393.4:c.355A>T MANE Select	ENSP00000241393.3:p.Asn119Tyr
ENST00000241393.3:c.355A>T	ENSP00000241393.3:p.Asn119Tyr
ENST00000409817.1:c.367A>T	ENSP00000386884.1:p.Asn123Tyr
ENST00000466288.1:n.549A>T
NM_001008540.1:c.367A>T	NP_001008540.1:p.Asn123Tyr
NM_003467.2:c.355A>T , LRG_51t1:c.355A>T	NP_003458.1:p.Asn119Tyr
NM_001008540.2:c.367A>T	NP_001008540.1:p.Asn123Tyr
NM_001348056.1:c.568A>T	NP_001334985.1:p.Asn190Tyr
NM_001348059.1:c.454A>T	NP_001334988.1:p.Asn152Tyr
NM_001348060.1:c.310A>T	NP_001334989.1:p.Asn104Tyr
NM_001348056.2:c.568A>T	NP_001334985.1:p.Asn190Tyr
NM_001348059.2:c.454A>T	NP_001334988.1:p.Asn152Tyr
NM_001348060.2:c.310A>T	NP_001334989.1:p.Asn104Tyr
NM_003467.3:c.355A>T MANE Select	NP_003458.1:p.Asn119Tyr