Canonical Allele Identifier: CA348659614

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873166G>A (hg19) ; chr2:g.136115596G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115596G>A , CM000664.2:g.136115596G>A	GRCh38
NC_000002.11:g.136873166G>A , CM000664.1:g.136873166G>A	GRCh37
NC_000002.10:g.136589636G>A	NCBI36
NG_011587.1:g.7560C>T , LRG_51:g.7560C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.320C>T	ENSP00000512428.1:p.Ala107Val
ENST00000696137.1:c.287C>T	ENSP00000512429.1:p.Ala96Val
ENST00000696152.1:c.287C>T	ENSP00000512443.1:p.Ala96Val
ENST00000696228.1:c.320C>T	ENSP00000512494.1:p.Ala107Val
ENST00000241393.4:c.332C>T MANE Select	ENSP00000241393.3:p.Ala111Val
ENST00000241393.3:c.332C>T	ENSP00000241393.3:p.Ala111Val
ENST00000409817.1:c.344C>T	ENSP00000386884.1:p.Ala115Val
ENST00000466288.1:n.526C>T
NM_001008540.1:c.344C>T	NP_001008540.1:p.Ala115Val
NM_003467.2:c.332C>T , LRG_51t1:c.332C>T	NP_003458.1:p.Ala111Val
NM_001008540.2:c.344C>T	NP_001008540.1:p.Ala115Val
NM_001348056.1:c.545C>T	NP_001334985.1:p.Ala182Val
NM_001348059.1:c.431C>T	NP_001334988.1:p.Ala144Val
NM_001348060.1:c.287C>T	NP_001334989.1:p.Ala96Val
NM_001348056.2:c.545C>T	NP_001334985.1:p.Ala182Val
NM_001348059.2:c.431C>T	NP_001334988.1:p.Ala144Val
NM_001348060.2:c.287C>T	NP_001334989.1:p.Ala96Val
NM_003467.3:c.332C>T MANE Select	NP_003458.1:p.Ala111Val