Canonical Allele Identifier: CA429206424

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873165T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115595T>G , CM000664.2:g.136115595T>G	GRCh38
NC_000002.11:g.136873165T>G , CM000664.1:g.136873165T>G	GRCh37
NC_000002.10:g.136589635T>G	NCBI36
NG_011587.1:g.7561A>C , LRG_51:g.7561A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.321A>C	ENSP00000512428.1:p.Ala107=
ENST00000696137.1:c.288A>C	ENSP00000512429.1:p.Ala96=
ENST00000696152.1:c.288A>C	ENSP00000512443.1:p.Ala96=
ENST00000696228.1:c.321A>C	ENSP00000512494.1:p.Ala107=
ENST00000241393.4:c.333A>C MANE Select	ENSP00000241393.3:p.Ala111=
ENST00000241393.3:c.333A>C	ENSP00000241393.3:p.Ala111=
ENST00000409817.1:c.345A>C	ENSP00000386884.1:p.Ala115=
ENST00000466288.1:n.527A>C
NM_001008540.1:c.345A>C	NP_001008540.1:p.Ala115=
NM_003467.2:c.333A>C , LRG_51t1:c.333A>C	NP_003458.1:p.Ala111=
NM_001008540.2:c.345A>C	NP_001008540.1:p.Ala115=
NM_001348056.1:c.546A>C	NP_001334985.1:p.Ala182=
NM_001348059.1:c.432A>C	NP_001334988.1:p.Ala144=
NM_001348060.1:c.288A>C	NP_001334989.1:p.Ala96=
NM_001348056.2:c.546A>C	NP_001334985.1:p.Ala182=
NM_001348059.2:c.432A>C	NP_001334988.1:p.Ala144=
NM_001348060.2:c.288A>C	NP_001334989.1:p.Ala96=
NM_003467.3:c.333A>C MANE Select	NP_003458.1:p.Ala111=