Canonical Allele Identifier: CA1896229107

Gene: PIP4K2A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.22558510C= , CM000672.2:g.22558510C=	GRCh38
NC_000010.10:g.22847439C= , CM000672.1:g.22847439C=	GRCh37
NC_000010.9:g.22887445C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376573.9:c.679-7738G= MANE Select	ENSP00000365757.4:n.679-7738G=
ENST00000323883.11:c.259-7738G=	ENSP00000326294.7:n.259-7738G=
ENST00000376573.8:c.679-7738G=	ENSP00000365757.4:n.679-7738G=
ENST00000545335.5:c.502-7738G=	ENSP00000442098.1:n.502-7738G=
ENST00000604912.1:c.217-7738G=	ENSP00000473858.1:n.217-7738G=
NM_005028.4:c.679-7738G=	NP_005019.2:n.679-7738G=
XM_006717450.2:c.526-7738G=	XP_006717513.1:n.526-7738G=
XM_011519494.1:c.640-7738G=	XP_011517796.1:n.640-7738G=
XM_011519495.1:c.592-7738G=	XP_011517797.1:n.592-7738G=
XM_011519496.1:c.502-7738G=	XP_011517798.1:n.502-7738G=
NM_001330062.1:c.502-7738G=	NP_001316991.1:n.502-7738G=
XM_017016330.1:c.502-7738G=	XP_016871819.1:n.502-7738G=
XM_017016331.1:c.502-7738G=	XP_016871820.1:n.502-7738G=
XM_017016332.1:c.349-7738G=	XP_016871821.1:n.349-7738G=
NM_005028.5:c.679-7738G= MANE Select	NP_005019.2:n.679-7738G=
NM_001330062.2:c.502-7738G=	NP_001316991.1:n.502-7738G=