Canonical Allele Identifier: CA1896221598

Gene: PIP4K2A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.22550699T= , CM000672.2:g.22550699T=	GRCh38
NC_000010.10:g.22839628T= , CM000672.1:g.22839628T=	GRCh37
NC_000010.9:g.22879634T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005028.5:c.752A= MANE Select	NP_005019.2:p.Asn251=
ENST00000376573.9:c.752A= MANE Select	ENSP00000365757.4:p.Asn251=
NM_001330062.1:c.575A=	NP_001316991.1:p.Asn192=
NM_001330062.2:c.575A=	NP_001316991.1:p.Asn192=
NM_005028.4:c.752A=	NP_005019.2:p.Asn251=
ENST00000323883.11:c.332A=	ENSP00000326294.7:p.Asn111=
ENST00000376573.8:c.752A=	ENSP00000365757.4:p.Asn251=
ENST00000545335.5:c.575A=	ENSP00000442098.1:p.Asn192=
ENST00000604912.1:c.290A=	ENSP00000473858.1:p.Asn97=
XM_006717450.2:c.599A=	XP_006717513.1:p.Asn200=
XM_011519494.1:c.713A=	XP_011517796.1:p.Asn238=
XM_011519495.1:c.665A=	XP_011517797.1:p.Asn222=
XM_011519496.1:c.575A=	XP_011517798.1:p.Asn192=
XM_017016330.1:c.575A=	XP_016871819.1:p.Asn192=
XM_017016331.1:c.575A=	XP_016871820.1:p.Asn192=
XM_017016332.1:c.422A=	XP_016871821.1:p.Asn141=