Canonical Allele Identifier: CA929120779
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1838802439

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531617_62531618insAAAAT , CM000672.2:g.62531617_62531618insAAAAT GRCh38
NC_000010.10:g.64291376_64291377insAAAAT , CM000672.1:g.64291376_64291377insAAAAT GRCh37
NC_000010.9:g.63961382_63961383insAAAAT NCBI36
NG_021209.1:g.162461_162462insAAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71820_981+71821insAAAAT ENSP00000502188.1:n.981+71820_981+71821insAAAAT
ENST00000395251.5:c.-185+11020_-185+11021insAAAAT ENSP00000378672.1:n.-185+11020_-185+11021insAAAAT
ENST00000410046.7:c.981+71820_981+71821insAAAAT ENSP00000387091.3:n.981+71820_981+71821insAAAAT
NM_199451.2:c.981+71820_981+71821insAAAAT NP_955523.1:n.981+71820_981+71821insAAAAT
NM_199452.3:c.-185+11020_-185+11021insAAAAT NP_955524.3:n.-185+11020_-185+11021insAAAAT
XM_017015937.2:c.982-12592_982-12591insAAAAT XP_016871426.1:n.982-12592_982-12591insAAAAT
NM_199451.3:c.981+71820_981+71821insAAAAT NP_955523.1:n.981+71820_981+71821insAAAAT