Canonical Allele Identifier: CA2258782477

Gene: PIP4K2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.38765943A= , CM000679.2:g.38765943A=	GRCh38
NC_000017.10:g.36922196A= , CM000679.1:g.36922196A=	GRCh37
NC_000017.9:g.34175722A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619039.5:c.*3748T= MANE Select	ENSP00000482548.1:n.*3748T=
ENST00000619039.4:c.*3748T=	ENSP00000482548.1:n.*3748T=
NM_003559.4:c.*3748T=	NP_003550.1:n.*3748T=
XM_011525326.1:c.*3748T=	XP_011523628.1:n.*3748T=
XM_011525327.1:c.*3748T=	XP_011523629.1:n.*3748T=
XM_011525328.1:c.*3748T=	XP_011523630.1:n.*3748T=
XM_011525330.1:c.*3748T=	XP_011523632.1:n.*3748T=
XM_011525331.1:c.*3748T=	XP_011523633.1:n.*3748T=
XM_011525326.3:c.*3748T=	XP_011523628.1:n.*3748T=
XM_011525327.2:c.*3748T=	XP_011523629.1:n.*3748T=
XM_011525330.2:c.*3748T=	XP_011523632.1:n.*3748T=
XM_017025197.1:c.*3748T=	XP_016880686.1:n.*3748T=
XM_017025199.1:c.*3748T=	XP_016880688.1:n.*3748T=
NM_003559.5:c.*3748T= MANE Select	NP_003550.1:n.*3748T=