Canonical Allele Identifier: CA2326929175

Gene: PBX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19610913G= , CM000681.2:g.19610913G=	GRCh38
NC_000019.9:g.19721722G= , CM000681.1:g.19721722G=	GRCh37
NC_000019.8:g.19582722G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025245.3:c.119+7598C= MANE Select	NP_079521.1:n.119+7598C=
ENST00000251203.14:c.119+7598C= MANE Select	ENSP00000251203.5:n.119+7598C=
NM_025245.2:c.119+7598C=	NP_079521.1:n.119+7598C=
NR_038198.1:n.406+7598C=
NR_038198.2:n.177+7598C=
ENST00000251203.13:c.119+7598C=	ENSP00000251203.5:n.119+7598C=
ENST00000557978.6:c.119+7598C=	ENSP00000453348.1:n.119+7598C=
ENST00000558222.1:c.119+7598C=	ENSP00000453069.1:n.119+7598C=
XM_006722911.2:c.-104+7598C=	XP_006722974.1:n.-104+7598C=
XM_006722911.3:c.-104+7598C=	XP_006722974.1:n.-104+7598C=
XM_011528320.1:c.119+7598C=	XP_011526622.1:n.119+7598C=
XM_011528320.3:c.119+7598C=	XP_011526622.1:n.119+7598C=
XM_011528321.1:c.119+7598C=	XP_011526623.1:n.119+7598C=
XM_011528323.1:c.119+7598C=	XP_011526625.1:n.119+7598C=
XM_017027330.2:c.119+7598C=	XP_016882819.1:n.119+7598C=
XR_001753767.2:n.174+7598C=
XR_936206.1:n.401+7598C=