Canonical Allele Identifier: CA929120485
Gene: ZNF365 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531324_62531325insG , CM000672.2:g.62531324_62531325insG GRCh38
NC_000010.10:g.64291083_64291084insG , CM000672.1:g.64291083_64291084insG GRCh37
NC_000010.9:g.63961089_63961090insG NCBI36
NG_021209.1:g.162168_162169insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71527_981+71528insG ENSP00000502188.1:n.981+71527_981+71528insG
ENST00000395251.5:c.-185+10727_-185+10728insG ENSP00000378672.1:n.-185+10727_-185+10728insG
ENST00000410046.7:c.981+71527_981+71528insG ENSP00000387091.3:n.981+71527_981+71528insG
NM_199451.2:c.981+71527_981+71528insG NP_955523.1:n.981+71527_981+71528insG
NM_199452.3:c.-185+10727_-185+10728insG NP_955524.3:n.-185+10727_-185+10728insG
XM_017015937.2:c.982-12885_982-12884insG XP_016871426.1:n.982-12885_982-12884insG
NM_199451.3:c.981+71527_981+71528insG NP_955523.1:n.981+71527_981+71528insG