Canonical Allele Identifier: CA16609493
Gene: ZNF462 HGNC NCBI

Linked Data

ClinVar Variation Id: 402118
dbSNP Id: rs1060499550

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.106926891_106926892delinsA , CM000671.2:g.106926891_106926892delinsA GRCh38
NC_000009.11:g.109689172_109689173delinsA , CM000671.1:g.109689172_109689173delinsA GRCh37
NC_000009.10:g.108728993_108728994delinsA NCBI36
NG_052913.1:g.68795_68796delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000277225.10:c.2979_2980delinsA MANE Select ENSP00000277225.5:p.Val994TrpfsTer?
ENST00000277225.9:c.2979_2980delinsA ENSP00000277225.5:p.Val994TrpfsTer?
ENST00000472574.1:c.280+2699_280+2700delinsA ENSP00000476222.1:n.280+2699_280+2700deli...
NM_021224.4:c.2979_2980delinsA NP_067047.4:p.Val994TrpfsTer?
XM_006717209.2:c.2979_2980delinsA XP_006717272.1:p.Val994TrpfsTer?
XM_006717210.2:c.2979_2980delinsA XP_006717273.1:p.Val994TrpfsTer?
XM_006717211.2:c.2979_2980delinsA XP_006717274.1:p.Val994TrpfsTer?
XM_006717212.2:c.2979_2980delinsA XP_006717275.1:p.Val994TrpfsTer?
XM_006717215.2:c.2979_2980delinsA XP_006717278.1:p.Val994TrpfsTer?
XM_006717216.2:c.2979_2980delinsA XP_006717279.1:p.Val994TrpfsTer?
XM_006717218.2:c.2979_2980delinsA XP_006717281.1:p.Val994TrpfsTer?
XM_011518892.1:c.2979_2980delinsA XP_011517194.1:p.Val994TrpfsTer?
NM_001347997.1:c.2979_2980delinsA NP_001334926.1:p.Val994TrpfsTer?
NM_021224.5:c.2979_2980delinsA NP_067047.4:p.Val994TrpfsTer?
XM_006717209.4:c.2979_2980delinsA XP_006717272.1:p.Val994TrpfsTer?
XM_006717211.4:c.2979_2980delinsA XP_006717274.1:p.Val994TrpfsTer?
XM_006717212.4:c.2979_2980delinsA XP_006717275.1:p.Val994TrpfsTer?
XM_006717215.4:c.2979_2980delinsA XP_006717278.1:p.Val994TrpfsTer?
XM_006717216.4:c.2979_2980delinsA XP_006717279.1:p.Val994TrpfsTer?
XM_006717218.4:c.2979_2980delinsA XP_006717281.1:p.Val994TrpfsTer?
XM_017014996.2:c.2979_2980delinsA XP_016870485.1:p.Val994TrpfsTer?
XM_017014997.2:c.2979_2980delinsA XP_016870486.1:p.Val994TrpfsTer?
XM_017014998.2:c.2979_2980delinsA XP_016870487.1:p.Val994TrpfsTer?
XM_024447629.1:c.2979_2980delinsA XP_024303397.1:p.Val994TrpfsTer?
NM_021224.6:c.2979_2980delinsA MANE Select NP_067047.4:p.Val994TrpfsTer?
NM_001347997.2:c.2979_2980delinsA NP_001334926.1:p.Val994TrpfsTer?