Canonical Allele Identifier: CA1914566332
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1841382541

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62492143_62492146del , CM000672.2:g.62492143_62492146del GRCh38
NC_000010.10:g.64251902_64251905del , CM000672.1:g.64251902_64251905del GRCh37
NC_000010.9:g.63921908_63921911del NCBI36
NG_021209.1:g.122987_122990del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+32346_981+32349del ENSP00000502188.1:n.981+32346_981+32349del
ENST00000410046.7:c.981+32346_981+32349del ENSP00000387091.3:n.981+32346_981+32349del
NM_199451.2:c.981+32346_981+32349del NP_955523.1:n.981+32346_981+32349del
XM_017015937.2:c.981+32346_981+32349del XP_016871426.1:n.981+32346_981+32349del
NM_199451.3:c.981+32346_981+32349del NP_955523.1:n.981+32346_981+32349del