Canonical Allele Identifier: CA429206746

Gene: CXCR4

Linked Data

• ClinVar Variation Id: 1995877
• ClinVar RCV Id: RCV002801627
• MyVariant Identifiers: chr2:g.136873156G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115586G>T , CM000664.2:g.136115586G>T	GRCh38
NC_000002.11:g.136873156G>T , CM000664.1:g.136873156G>T	GRCh37
NC_000002.10:g.136589626G>T	NCBI36
NG_011587.1:g.7570C>A , LRG_51:g.7570C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.330C>A	ENSP00000512428.1:p.Val110=
ENST00000696137.1:c.297C>A	ENSP00000512429.1:p.Val99=
ENST00000696152.1:c.297C>A	ENSP00000512443.1:p.Val99=
ENST00000696228.1:c.330C>A	ENSP00000512494.1:p.Val110=
ENST00000241393.4:c.342C>A MANE Select	ENSP00000241393.3:p.Val114=
ENST00000241393.3:c.342C>A	ENSP00000241393.3:p.Val114=
ENST00000409817.1:c.354C>A	ENSP00000386884.1:p.Val118=
ENST00000466288.1:n.536C>A
NM_001008540.1:c.354C>A	NP_001008540.1:p.Val118=
NM_003467.2:c.342C>A , LRG_51t1:c.342C>A	NP_003458.1:p.Val114=
NM_001008540.2:c.354C>A	NP_001008540.1:p.Val118=
NM_001348056.1:c.555C>A	NP_001334985.1:p.Val185=
NM_001348059.1:c.441C>A	NP_001334988.1:p.Val147=
NM_001348060.1:c.297C>A	NP_001334989.1:p.Val99=
NM_001348056.2:c.555C>A	NP_001334985.1:p.Val185=
NM_001348059.2:c.441C>A	NP_001334988.1:p.Val147=
NM_001348060.2:c.297C>A	NP_001334989.1:p.Val99=
NM_003467.3:c.342C>A MANE Select	NP_003458.1:p.Val114=