Canonical Allele Identifier: CA429206636

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873096G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115526G>C , CM000664.2:g.136115526G>C	GRCh38
NC_000002.11:g.136873096G>C , CM000664.1:g.136873096G>C	GRCh37
NC_000002.10:g.136589566G>C	NCBI36
NG_011587.1:g.7630C>G , LRG_51:g.7630C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.390C>G	ENSP00000512428.1:p.Arg130=
ENST00000696137.1:c.357C>G	ENSP00000512429.1:p.Arg119=
ENST00000696152.1:c.357C>G	ENSP00000512443.1:p.Arg119=
ENST00000696228.1:c.390C>G	ENSP00000512494.1:p.Arg130=
ENST00000241393.4:c.402C>G MANE Select	ENSP00000241393.3:p.Arg134=
ENST00000241393.3:c.402C>G	ENSP00000241393.3:p.Arg134=
ENST00000409817.1:c.414C>G	ENSP00000386884.1:p.Arg138=
ENST00000466288.1:n.596C>G
NM_001008540.1:c.414C>G	NP_001008540.1:p.Arg138=
NM_003467.2:c.402C>G , LRG_51t1:c.402C>G	NP_003458.1:p.Arg134=
NM_001008540.2:c.414C>G	NP_001008540.1:p.Arg138=
NM_001348056.1:c.615C>G	NP_001334985.1:p.Arg205=
NM_001348059.1:c.501C>G	NP_001334988.1:p.Arg167=
NM_001348060.1:c.357C>G	NP_001334989.1:p.Arg119=
NM_001348056.2:c.615C>G	NP_001334985.1:p.Arg205=
NM_001348059.2:c.501C>G	NP_001334988.1:p.Arg167=
NM_001348060.2:c.357C>G	NP_001334989.1:p.Arg119=
NM_003467.3:c.402C>G MANE Select	NP_003458.1:p.Arg134=