Canonical Allele Identifier: CA1399188596
Gene: ZNF148 HGNC NCBI

Linked Data

dbSNP Id: rs1935905250

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.125232641_125232642insC , CM000665.2:g.125232641_125232642insC GRCh38
NC_000003.11:g.124951485_124951486insC , CM000665.1:g.124951485_124951486insC GRCh37
NC_000003.10:g.126434175_126434176insC NCBI36
NG_052987.1:g.147713_147714insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000471196.2:c.2084_2085insG ENSP00000420038.2:p.Asn695LysfsTer22
ENST00000700044.1:c.2084_2085insG ENSP00000514760.1:p.Asn695LysfsTer22
ENST00000360647.9:c.2084_2085insG MANE Select ENSP00000353863.4:p.Asn695LysfsTer22
ENST00000360647.8:c.2084_2085insG ENSP00000353863.4:p.Asn695LysfsTer22
ENST00000468369.5:c.134_135insG ENSP00000420102.1:p.Asn45LysfsTer22
ENST00000484491.5:c.2084_2085insG ENSP00000420335.1:p.Asn695LysfsTer22
ENST00000485866.5:c.2084_2085insG ENSP00000420448.1:p.Asn695LysfsTer22
ENST00000492394.5:c.2084_2085insG ENSP00000419322.1:p.Asn695LysfsTer22
ENST00000496732.1:n.186_187insG
ENST00000497929.1:n.2080_2081insG
NM_021964.2:c.2084_2085insG NP_068799.2:p.Asn695LysfsTer22
NM_001348424.1:c.2084_2085insG NP_001335353.1:p.Asn695LysfsTer22
NM_001348425.2:c.2084_2085insG NP_001335354.1:p.Asn695LysfsTer22
NM_001348426.2:c.2084_2085insG NP_001335355.1:p.Asn695LysfsTer22
NM_001348427.2:c.2084_2085insG NP_001335356.1:p.Asn695LysfsTer22
NM_001348428.2:c.2084_2085insG NP_001335357.1:p.Asn695LysfsTer22
NM_001348429.2:c.2084_2085insG NP_001335358.1:p.Asn695LysfsTer22
NM_001348430.2:c.2084_2085insG NP_001335359.1:p.Asn695LysfsTer22
NM_001348431.2:c.2084_2085insG NP_001335360.1:p.Asn695LysfsTer22
NM_001348432.2:c.2084_2085insG NP_001335361.1:p.Asn695LysfsTer22
NM_001348433.2:c.2084_2085insG NP_001335362.1:p.Asn695LysfsTer22
NM_001348434.2:c.1958_1959insG NP_001335363.1:p.Asn653LysfsTer22
NM_021964.3:c.2084_2085insG MANE Select NP_068799.2:p.Asn695LysfsTer22