Canonical Allele Identifier: CA929119560
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs5785531

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528650_62528653del , CM000672.2:g.62528650_62528653del GRCh38
NC_000010.10:g.64288409_64288412del , CM000672.1:g.64288409_64288412del GRCh37
NC_000010.9:g.63958415_63958418del NCBI36
NG_021209.1:g.159494_159497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+68853_981+68856del ENSP00000502188.1:n.981+68853_981+68856del
ENST00000395251.5:c.-185+8053_-185+8056del ENSP00000378672.1:n.-185+8053_-185+8056del
ENST00000410046.7:c.981+68853_981+68856del ENSP00000387091.3:n.981+68853_981+68856del
NM_199451.2:c.981+68853_981+68856del NP_955523.1:n.981+68853_981+68856del
NM_199452.3:c.-185+8053_-185+8056del NP_955524.3:n.-185+8053_-185+8056del
XM_017015937.2:c.982-15559_982-15556del XP_016871426.1:n.982-15559_982-15556del
NM_199451.3:c.981+68853_981+68856del NP_955523.1:n.981+68853_981+68856del