Canonical Allele Identifier: CA1896202286

Gene: PIP4K2A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.22577893C= , CM000672.2:g.22577893C=	GRCh38
NC_000010.10:g.22866822C= , CM000672.1:g.22866822C=	GRCh37
NC_000010.9:g.22906828C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376573.9:c.493-4436G= MANE Select	ENSP00000365757.4:n.493-4436G=
ENST00000323883.11:c.31-4436G=	ENSP00000326294.7:n.31-4436G=
ENST00000376573.8:c.493-4436G=	ENSP00000365757.4:n.493-4436G=
ENST00000422321.5:n.349-4436G=
ENST00000545335.5:c.316-4436G=	ENSP00000442098.1:n.316-4436G=
ENST00000604912.1:c.31-4436G=	ENSP00000473858.1:n.31-4436G=
NM_005028.4:c.493-4436G=	NP_005019.2:n.493-4436G=
XM_006717450.2:c.340-4436G=	XP_006717513.1:n.340-4436G=
XM_011519494.1:c.493-4436G=	XP_011517796.1:n.493-4436G=
XM_011519495.1:c.406-4436G=	XP_011517797.1:n.406-4436G=
XM_011519496.1:c.316-4436G=	XP_011517798.1:n.316-4436G=
XM_011519497.1:c.493-4436G=	XP_011517799.1:n.493-4436G=
NM_001330062.1:c.316-4436G=	NP_001316991.1:n.316-4436G=
XM_017016330.1:c.316-4436G=	XP_016871819.1:n.316-4436G=
XM_017016331.1:c.316-4436G=	XP_016871820.1:n.316-4436G=
XM_017016332.1:c.163-4436G=	XP_016871821.1:n.163-4436G=
NM_005028.5:c.493-4436G= MANE Select	NP_005019.2:n.493-4436G=
NM_001330062.2:c.316-4436G=	NP_001316991.1:n.316-4436G=