Canonical Allele Identifier: CA348659288

Gene: CXCR4

Linked Data

• MyVariant Identifiers: chr2:g.136873111G>C (hg19) ; chr2:g.136115541G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115541G>C , CM000664.2:g.136115541G>C	GRCh38
NC_000002.11:g.136873111G>C , CM000664.1:g.136873111G>C	GRCh37
NC_000002.10:g.136589581G>C	NCBI36
NG_011587.1:g.7615C>G , LRG_51:g.7615C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.375C>G	ENSP00000512428.1:p.Phe125Leu
ENST00000696137.1:c.342C>G	ENSP00000512429.1:p.Phe114Leu
ENST00000696152.1:c.342C>G	ENSP00000512443.1:p.Phe114Leu
ENST00000696228.1:c.375C>G	ENSP00000512494.1:p.Phe125Leu
ENST00000241393.4:c.387C>G MANE Select	ENSP00000241393.3:p.Phe129Leu
ENST00000241393.3:c.387C>G	ENSP00000241393.3:p.Phe129Leu
ENST00000409817.1:c.399C>G	ENSP00000386884.1:p.Phe133Leu
ENST00000466288.1:n.581C>G
NM_001008540.1:c.399C>G	NP_001008540.1:p.Phe133Leu
NM_003467.2:c.387C>G , LRG_51t1:c.387C>G	NP_003458.1:p.Phe129Leu
NM_001008540.2:c.399C>G	NP_001008540.1:p.Phe133Leu
NM_001348056.1:c.600C>G	NP_001334985.1:p.Phe200Leu
NM_001348059.1:c.486C>G	NP_001334988.1:p.Phe162Leu
NM_001348060.1:c.342C>G	NP_001334989.1:p.Phe114Leu
NM_001348056.2:c.600C>G	NP_001334985.1:p.Phe200Leu
NM_001348059.2:c.486C>G	NP_001334988.1:p.Phe162Leu
NM_001348060.2:c.342C>G	NP_001334989.1:p.Phe114Leu
NM_003467.3:c.387C>G MANE Select	NP_003458.1:p.Phe129Leu