Canonical Allele Identifier: CA354294280
Gene: ZNF148 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.125232819G>T , CM000665.2:g.125232819G>T GRCh38
NC_000003.11:g.124951663G>T , CM000665.1:g.124951663G>T GRCh37
NC_000003.10:g.126434353G>T NCBI36
NG_052987.1:g.147536C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000471196.2:c.1907C>A ENSP00000420038.2:p.Thr636Asn
ENST00000700044.1:c.1907C>A ENSP00000514760.1:p.Thr636Asn
ENST00000360647.9:c.1907C>A MANE Select ENSP00000353863.4:p.Thr636Asn
ENST00000360647.8:c.1907C>A ENSP00000353863.4:p.Thr636Asn
ENST00000468369.5:c.122-165C>A ENSP00000420102.1:n.122-165C>A
ENST00000484491.5:c.1907C>A ENSP00000420335.1:p.Thr636Asn
ENST00000485866.5:c.1907C>A ENSP00000420448.1:p.Thr636Asn
ENST00000492394.5:c.1907C>A ENSP00000419322.1:p.Thr636Asn
ENST00000496732.1:n.174-165C>A
ENST00000497929.1:n.1903C>A
ENST00000544464.5:c.*540C>A ENSP00000437916.2:n.*540C>A
NM_021964.2:c.1907C>A NP_068799.2:p.Thr636Asn
NM_001348424.1:c.1907C>A NP_001335353.1:p.Thr636Asn
NM_001348425.2:c.1907C>A NP_001335354.1:p.Thr636Asn
NM_001348426.2:c.1907C>A NP_001335355.1:p.Thr636Asn
NM_001348427.2:c.1907C>A NP_001335356.1:p.Thr636Asn
NM_001348428.2:c.1907C>A NP_001335357.1:p.Thr636Asn
NM_001348429.2:c.1907C>A NP_001335358.1:p.Thr636Asn
NM_001348430.2:c.1907C>A NP_001335359.1:p.Thr636Asn
NM_001348431.2:c.1907C>A NP_001335360.1:p.Thr636Asn
NM_001348432.2:c.1907C>A NP_001335361.1:p.Thr636Asn
NM_001348433.2:c.1907C>A NP_001335362.1:p.Thr636Asn
NM_001348434.2:c.1781C>A NP_001335363.1:p.Thr594Asn
NM_021964.3:c.1907C>A MANE Select NP_068799.2:p.Thr636Asn