Canonical Allele Identifier: CA374409351
Gene: ZNF462 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.106928524C>T , CM000671.2:g.106928524C>T GRCh38
NC_000009.11:g.109690805C>T , CM000671.1:g.109690805C>T GRCh37
NC_000009.10:g.108730626C>T NCBI36
NG_052913.1:g.70428C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000277225.10:c.4612C>T MANE Select ENSP00000277225.5:p.His1538Tyr
ENST00000277225.9:c.4612C>T ENSP00000277225.5:p.His1538Tyr
ENST00000374686.6:c.1261C>T ENSP00000363818.2:p.His421Tyr
ENST00000441147.6:c.1147C>T ENSP00000397306.2:p.His383Tyr
ENST00000472574.1:c.281-2001C>T ENSP00000476222.1:n.281-2001C>T
ENST00000480607.5:n.240+1360C>T
NM_021224.4:c.4612C>T NP_067047.4:p.His1538Tyr
XM_006717209.2:c.4612C>T XP_006717272.1:p.His1538Tyr
XM_006717210.2:c.4612C>T XP_006717273.1:p.His1538Tyr
XM_006717211.2:c.4612C>T XP_006717274.1:p.His1538Tyr
XM_006717212.2:c.4612C>T XP_006717275.1:p.His1538Tyr
XM_006717215.2:c.4612C>T XP_006717278.1:p.His1538Tyr
XM_006717216.2:c.4612C>T XP_006717279.1:p.His1538Tyr
XM_006717218.2:c.3252+1360C>T XP_006717281.1:n.3252+1360C>T
XM_011518892.1:c.4612C>T XP_011517194.1:p.His1538Tyr
NM_001347997.1:c.3252+1360C>T NP_001334926.1:n.3252+1360C>T
NM_021224.5:c.4612C>T NP_067047.4:p.His1538Tyr
XM_006717209.4:c.4612C>T XP_006717272.1:p.His1538Tyr
XM_006717211.4:c.4612C>T XP_006717274.1:p.His1538Tyr
XM_006717212.4:c.4612C>T XP_006717275.1:p.His1538Tyr
XM_006717215.4:c.4612C>T XP_006717278.1:p.His1538Tyr
XM_006717216.4:c.4612C>T XP_006717279.1:p.His1538Tyr
XM_006717218.4:c.3252+1360C>T XP_006717281.1:n.3252+1360C>T
XM_017014996.2:c.4612C>T XP_016870485.1:p.His1538Tyr
XM_017014997.2:c.4612C>T XP_016870486.1:p.His1538Tyr
XM_017014998.2:c.3252+1360C>T XP_016870487.1:n.3252+1360C>T
XM_024447629.1:c.4612C>T XP_024303397.1:p.His1538Tyr
NM_021224.6:c.4612C>T MANE Select NP_067047.4:p.His1538Tyr
NM_001347997.2:c.3252+1360C>T NP_001334926.1:n.3252+1360C>T