Canonical Allele Identifier: CA7858347
Gene: ZNF205 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3120089C>T , CM000678.2:g.3120089C>T GRCh38
NC_000016.9:g.3170090C>T , CM000678.1:g.3170090C>T GRCh37
NC_000016.8:g.3110091C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001042428.2:c.1429C>T MANE Select NP_001035893.1:p.His477Tyr
ENST00000219091.9:c.1429C>T MANE Select ENSP00000219091.4:p.His477Tyr
NM_001042428.1:c.1429C>T NP_001035893.1:p.His477Tyr
NM_001278158.1:c.1429C>T NP_001265087.1:p.His477Tyr
NM_001278158.2:c.1429C>T NP_001265087.1:p.His477Tyr
NM_003456.2:c.1429C>T NP_003447.2:p.His477Tyr
NM_003456.3:c.1429C>T NP_003447.2:p.His477Tyr
ENST00000219091.8:c.1429C>T ENSP00000219091.4:p.His477Tyr
ENST00000382192.7:c.1429C>T ENSP00000371627.3:p.His477Tyr
ENST00000620094.4:c.1429C>T ENSP00000480401.1:p.His477Tyr
XM_005255558.1:c.1429C>T XP_005255615.1:p.His477Tyr
XM_005255558.2:c.1429C>T XP_005255615.1:p.His477Tyr