Canonical Allele Identifier: CA1290965875

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136114915G= , CM000664.2:g.136114915G=	GRCh38
NC_000002.11:g.136872485G= , CM000664.1:g.136872485G=	GRCh37
NC_000002.10:g.136588955G=	NCBI36
NG_011587.1:g.8241C= , LRG_51:g.8241C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003467.3:c.1013C= MANE Select	NP_003458.1:p.Ser338=
ENST00000241393.4:c.1013C= MANE Select	ENSP00000241393.3:p.Ser338=
NM_001008540.1:c.1025C=	NP_001008540.1:p.Ser342=
NM_001008540.2:c.1025C=	NP_001008540.1:p.Ser342=
NM_001348056.1:c.1226C=	NP_001334985.1:p.Ser409=
NM_001348056.2:c.1226C=	NP_001334985.1:p.Ser409=
NM_001348059.1:c.1112C=	NP_001334988.1:p.Ser371=
NM_001348059.2:c.1112C=	NP_001334988.1:p.Ser371=
NM_001348060.1:c.968C=	NP_001334989.1:p.Ser323=
NM_001348060.2:c.968C=	NP_001334989.1:p.Ser323=
NM_003467.2:c.1013C= , LRG_51t1:c.1013C=	NP_003458.1:p.Ser338=
ENST00000241393.3:c.1013C=	ENSP00000241393.3:p.Ser338=
ENST00000409817.1:c.1025C=	ENSP00000386884.1:p.Ser342=
ENST00000466288.1:n.1207C=
ENST00000696136.1:c.1001C=	ENSP00000512428.1:p.Ser334=
ENST00000696137.1:c.968C=	ENSP00000512429.1:p.Ser323=
ENST00000696152.1:c.968C=	ENSP00000512443.1:p.Ser323=
ENST00000696228.1:c.1001C=	ENSP00000512494.1:p.Ser334=