Canonical Allele Identifier: CA1399188673
Gene: ZNF148 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.125232710A= , CM000665.2:g.125232710A= GRCh38
NC_000003.11:g.124951554A= , CM000665.1:g.124951554A= GRCh37
NC_000003.10:g.126434244A= NCBI36
NG_052987.1:g.147645T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000471196.2:c.2016T= ENSP00000420038.2:p.Asp672=
ENST00000700044.1:c.2016T= ENSP00000514760.1:p.Asp672=
ENST00000360647.9:c.2016T= MANE Select ENSP00000353863.4:p.Asp672=
ENST00000360647.8:c.2016T= ENSP00000353863.4:p.Asp672=
ENST00000468369.5:c.122-56T= ENSP00000420102.1:n.122-56T=
ENST00000484491.5:c.2016T= ENSP00000420335.1:p.Asp672=
ENST00000485866.5:c.2016T= ENSP00000420448.1:p.Asp672=
ENST00000492394.5:c.2016T= ENSP00000419322.1:p.Asp672=
ENST00000496732.1:n.174-56T=
ENST00000497929.1:n.2012T=
NM_021964.2:c.2016T= NP_068799.2:p.Asp672=
NM_001348424.1:c.2016T= NP_001335353.1:p.Asp672=
NM_001348425.2:c.2016T= NP_001335354.1:p.Asp672=
NM_001348426.2:c.2016T= NP_001335355.1:p.Asp672=
NM_001348427.2:c.2016T= NP_001335356.1:p.Asp672=
NM_001348428.2:c.2016T= NP_001335357.1:p.Asp672=
NM_001348429.2:c.2016T= NP_001335358.1:p.Asp672=
NM_001348430.2:c.2016T= NP_001335359.1:p.Asp672=
NM_001348431.2:c.2016T= NP_001335360.1:p.Asp672=
NM_001348432.2:c.2016T= NP_001335361.1:p.Asp672=
NM_001348433.2:c.2016T= NP_001335362.1:p.Asp672=
NM_001348434.2:c.1890T= NP_001335363.1:p.Asp630=
NM_021964.3:c.2016T= MANE Select NP_068799.2:p.Asp672=