Canonical Allele Identifier: CA2339365
Community Standard Title: NM_207404.4(ZNF662):c.436C>T (p.Arg146Cys)
Gene: ZNF662 HGNC NCBI
KRBOX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42914509C>T , CM000665.2:g.42914509C>T GRCh38
NC_000003.11:g.42956001C>T , CM000665.1:g.42956001C>T GRCh37
NC_000003.10:g.42931005C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_207404.4:c.436C>T (ZNF662) MANE Select NP_997287.2:p.Arg146Cys
ENST00000440367.7:c.436C>T (ZNF662) MANE Select ENSP00000405047.2:p.Arg146Cys
NM_001134656.1:c.514C>T (ZNF662) NP_001128128.1:p.Arg172Cys
NM_001134656.2:c.514C>T (ZNF662) NP_001128128.1:p.Arg172Cys
NM_207404.3:c.436C>T (ZNF662) NP_997287.2:p.Arg146Cys
ENST00000328199.6:c.514C>T (ZNF662) ENSP00000329264.6:p.Arg172Cys
ENST00000422021.1:c.152-2940C>T (ZNF662) ENSP00000408945.1:n.152-2940C>T
ENST00000426937.5:c.-47+5600C>T (KRBOX1) ENSP00000413859.1:n.-47+5600C>T
ENST00000440367.6:c.436C>T (ZNF662) ENSP00000405047.2:p.Arg146Cys
ENST00000451200.6:n.169-24341C>T
ENST00000475386.1:n.1339C>T (ZNF662)