Canonical Allele Identifier: CA1896202288
Gene: PIP4K2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.22577902A= , CM000672.2:g.22577902A= GRCh38
NC_000010.10:g.22866831A= , CM000672.1:g.22866831A= GRCh37
NC_000010.9:g.22906837A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376573.9:c.493-4445T= MANE Select ENSP00000365757.4:n.493-4445T=
ENST00000323883.11:c.31-4445T= ENSP00000326294.7:n.31-4445T=
ENST00000376573.8:c.493-4445T= ENSP00000365757.4:n.493-4445T=
ENST00000422321.5:n.349-4445T=
ENST00000545335.5:c.316-4445T= ENSP00000442098.1:n.316-4445T=
ENST00000604912.1:c.31-4445T= ENSP00000473858.1:n.31-4445T=
NM_005028.4:c.493-4445T= NP_005019.2:n.493-4445T=
XM_006717450.2:c.340-4445T= XP_006717513.1:n.340-4445T=
XM_011519494.1:c.493-4445T= XP_011517796.1:n.493-4445T=
XM_011519495.1:c.406-4445T= XP_011517797.1:n.406-4445T=
XM_011519496.1:c.316-4445T= XP_011517798.1:n.316-4445T=
XM_011519497.1:c.493-4445T= XP_011517799.1:n.493-4445T=
NM_001330062.1:c.316-4445T= NP_001316991.1:n.316-4445T=
XM_017016330.1:c.316-4445T= XP_016871819.1:n.316-4445T=
XM_017016331.1:c.316-4445T= XP_016871820.1:n.316-4445T=
XM_017016332.1:c.163-4445T= XP_016871821.1:n.163-4445T=
NM_005028.5:c.493-4445T= MANE Select NP_005019.2:n.493-4445T=
NM_001330062.2:c.316-4445T= NP_001316991.1:n.316-4445T=