Canonical Allele Identifier: CA10654317
Community Standard Title: NM_001190417.2(ZNF674):c.*1120_*1121del
Gene: ZNF674 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46498722_46498723del , CM000685.2:g.46498722_46498723del GRCh38
NC_000023.10:g.46358157_46358158del , CM000685.1:g.46358157_46358158del GRCh37
NC_000023.9:g.46243101_46243102del NCBI36
NG_023376.1:g.51735_51736del
NG_023376.2:g.51735_51736del

Transcript Alleles

HGVS Amino-acid Change
NM_001190417.2:c.*1120_*1121del MANE Select NP_001177346.1:n.*1120_*1121del
ENST00000683375.1:c.*1120_*1121del MANE Select ENSP00000506769.1:n.*1120_*1121del
NM_001039891.2:c.*1120_*1121del NP_001034980.1:n.*1120_*1121del
NM_001039891.3:c.*1120_*1121del NP_001034980.1:n.*1120_*1121del
NM_001146291.1:c.*1120_*1121del NP_001139763.1:n.*1120_*1121del
NM_001146291.2:c.*1120_*1121del NP_001139763.1:n.*1120_*1121del
NM_001190417.1:c.*1120_*1121del NP_001177346.1:n.*1120_*1121del
ENST00000523374.5:c.*1120_*1121del ENSP00000429148.1:n.*1120_*1121del