Canonical Allele Identifier: CA1290966094

Gene: CXCR4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115604_136115610delinsTAGGAAG , CM000664.2:g.136115604_136115610delinsTAGGAAG	GRCh38
NC_000002.11:g.136873174_136873180delinsTAGGAAG , CM000664.1:g.136873174_136873180delinsTAGGAAG	GRCh37
NC_000002.10:g.136589644_136589650delinsTAGGAAG	NCBI36
NG_011587.1:g.7546_7552delinsCTTCCTA , LRG_51:g.7546_7552delinsCTTCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.306_312delinsCTTCCTA	ENSP00000512428.1:p.Asn102=
ENST00000696137.1:c.273_279delinsCTTCCTA	ENSP00000512429.1:p.Asn91=
ENST00000696152.1:c.273_279delinsCTTCCTA	ENSP00000512443.1:p.Asn91=
ENST00000696228.1:c.306_312delinsCTTCCTA	ENSP00000512494.1:p.Asn102=
ENST00000241393.4:c.318_324delinsCTTCCTA MANE Select	ENSP00000241393.3:p.Asn106=
ENST00000241393.3:c.318_324delinsCTTCCTA	ENSP00000241393.3:p.Asn106=
ENST00000409817.1:c.330_336delinsCTTCCTA	ENSP00000386884.1:p.Asn110=
ENST00000466288.1:n.512_518delinsCTTCCTA
NM_001008540.1:c.330_336delinsCTTCCTA	NP_001008540.1:p.Asn110=
NM_003467.2:c.318_324delinsCTTCCTA , LRG_51t1:c.318_324delinsCTTCCTA	NP_003458.1:p.Asn106=
NM_001008540.2:c.330_336delinsCTTCCTA	NP_001008540.1:p.Asn110=
NM_001348056.1:c.531_537delinsCTTCCTA	NP_001334985.1:p.Asn177=
NM_001348059.1:c.417_423delinsCTTCCTA	NP_001334988.1:p.Asn139=
NM_001348060.1:c.273_279delinsCTTCCTA	NP_001334989.1:p.Asn91=
NM_001348056.2:c.531_537delinsCTTCCTA	NP_001334985.1:p.Asn177=
NM_001348059.2:c.417_423delinsCTTCCTA	NP_001334988.1:p.Asn139=
NM_001348060.2:c.273_279delinsCTTCCTA	NP_001334989.1:p.Asn91=
NM_003467.3:c.318_324delinsCTTCCTA MANE Select	NP_003458.1:p.Asn106=