Canonical Allele Identifier: CA348659173

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873086T>A (hg19) ; chr2:g.136115516T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115516T>A , CM000664.2:g.136115516T>A	GRCh38
NC_000002.11:g.136873086T>A , CM000664.1:g.136873086T>A	GRCh37
NC_000002.10:g.136589556T>A	NCBI36
NG_011587.1:g.7640A>T , LRG_51:g.7640A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.400A>T	ENSP00000512428.1:p.Ile134Phe
ENST00000696137.1:c.367A>T	ENSP00000512429.1:p.Ile123Phe
ENST00000696152.1:c.367A>T	ENSP00000512443.1:p.Ile123Phe
ENST00000696228.1:c.400A>T	ENSP00000512494.1:p.Ile134Phe
ENST00000241393.4:c.412A>T MANE Select	ENSP00000241393.3:p.Ile138Phe
ENST00000241393.3:c.412A>T	ENSP00000241393.3:p.Ile138Phe
ENST00000409817.1:c.424A>T	ENSP00000386884.1:p.Ile142Phe
ENST00000466288.1:n.606A>T
NM_001008540.1:c.424A>T	NP_001008540.1:p.Ile142Phe
NM_003467.2:c.412A>T , LRG_51t1:c.412A>T	NP_003458.1:p.Ile138Phe
NM_001008540.2:c.424A>T	NP_001008540.1:p.Ile142Phe
NM_001348056.1:c.625A>T	NP_001334985.1:p.Ile209Phe
NM_001348059.1:c.511A>T	NP_001334988.1:p.Ile171Phe
NM_001348060.1:c.367A>T	NP_001334989.1:p.Ile123Phe
NM_001348056.2:c.625A>T	NP_001334985.1:p.Ile209Phe
NM_001348059.2:c.511A>T	NP_001334988.1:p.Ile171Phe
NM_001348060.2:c.367A>T	NP_001334989.1:p.Ile123Phe
NM_003467.3:c.412A>T MANE Select	NP_003458.1:p.Ile138Phe