Canonical Allele Identifier: CA429206609

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873090C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115520C>A , CM000664.2:g.136115520C>A	GRCh38
NC_000002.11:g.136873090C>A , CM000664.1:g.136873090C>A	GRCh37
NC_000002.10:g.136589560C>A	NCBI36
NG_011587.1:g.7636G>T , LRG_51:g.7636G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696136.1:c.396G>T	ENSP00000512428.1:p.Leu132=
ENST00000696137.1:c.363G>T	ENSP00000512429.1:p.Leu121=
ENST00000696152.1:c.363G>T	ENSP00000512443.1:p.Leu121=
ENST00000696228.1:c.396G>T	ENSP00000512494.1:p.Leu132=
ENST00000241393.4:c.408G>T MANE Select	ENSP00000241393.3:p.Leu136=
ENST00000241393.3:c.408G>T	ENSP00000241393.3:p.Leu136=
ENST00000409817.1:c.420G>T	ENSP00000386884.1:p.Leu140=
ENST00000466288.1:n.602G>T
NM_001008540.1:c.420G>T	NP_001008540.1:p.Leu140=
NM_003467.2:c.408G>T , LRG_51t1:c.408G>T	NP_003458.1:p.Leu136=
NM_001008540.2:c.420G>T	NP_001008540.1:p.Leu140=
NM_001348056.1:c.621G>T	NP_001334985.1:p.Leu207=
NM_001348059.1:c.507G>T	NP_001334988.1:p.Leu169=
NM_001348060.1:c.363G>T	NP_001334989.1:p.Leu121=
NM_001348056.2:c.621G>T	NP_001334985.1:p.Leu207=
NM_001348059.2:c.507G>T	NP_001334988.1:p.Leu169=
NM_001348060.2:c.363G>T	NP_001334989.1:p.Leu121=
NM_003467.3:c.408G>T MANE Select	NP_003458.1:p.Leu136=