Canonical Allele Identifier: CA1053149045
Gene: ZNF148 HGNC NCBI

Linked Data

dbSNP Id: rs1935905714

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.125232643_125232644insCCC , CM000665.2:g.125232643_125232644insCCC GRCh38
NC_000003.11:g.124951487_124951488insCCC , CM000665.1:g.124951487_124951488insCCC GRCh37
NC_000003.10:g.126434177_126434178insCCC NCBI36
NG_052987.1:g.147711_147712insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000471196.2:c.2082_2083insGGG ENSP00000420038.2:p.Thr694_Asn695insGly
ENST00000700044.1:c.2082_2083insGGG ENSP00000514760.1:p.Thr694_Asn695insGly
ENST00000360647.9:c.2082_2083insGGG MANE Select ENSP00000353863.4:p.Thr694_Asn695insGly
ENST00000360647.8:c.2082_2083insGGG ENSP00000353863.4:p.Thr694_Asn695insGly
ENST00000468369.5:c.132_133insGGG ENSP00000420102.1:p.Thr44_Asn45insGly
ENST00000484491.5:c.2082_2083insGGG ENSP00000420335.1:p.Thr694_Asn695insGly
ENST00000485866.5:c.2082_2083insGGG ENSP00000420448.1:p.Thr694_Asn695insGly
ENST00000492394.5:c.2082_2083insGGG ENSP00000419322.1:p.Thr694_Asn695insGly
ENST00000496732.1:n.184_185insGGG
ENST00000497929.1:n.2078_2079insGGG
NM_021964.2:c.2082_2083insGGG NP_068799.2:p.Thr694_Asn695insGly
NM_001348424.1:c.2082_2083insGGG NP_001335353.1:p.Thr694_Asn695insGly
NM_001348425.2:c.2082_2083insGGG NP_001335354.1:p.Thr694_Asn695insGly
NM_001348426.2:c.2082_2083insGGG NP_001335355.1:p.Thr694_Asn695insGly
NM_001348427.2:c.2082_2083insGGG NP_001335356.1:p.Thr694_Asn695insGly
NM_001348428.2:c.2082_2083insGGG NP_001335357.1:p.Thr694_Asn695insGly
NM_001348429.2:c.2082_2083insGGG NP_001335358.1:p.Thr694_Asn695insGly
NM_001348430.2:c.2082_2083insGGG NP_001335359.1:p.Thr694_Asn695insGly
NM_001348431.2:c.2082_2083insGGG NP_001335360.1:p.Thr694_Asn695insGly
NM_001348432.2:c.2082_2083insGGG NP_001335361.1:p.Thr694_Asn695insGly
NM_001348433.2:c.2082_2083insGGG NP_001335362.1:p.Thr694_Asn695insGly
NM_001348434.2:c.1956_1957insGGG NP_001335363.1:p.Thr652_Asn653insGly
NM_021964.3:c.2082_2083insGGG MANE Select NP_068799.2:p.Thr694_Asn695insGly