Canonical Allele Identifier: CA667275107

Gene: ZNF365

Linked Data

• dbSNP Id: rs1339011071
• gnomAD v3: 10-62528651-A-AG
• gnomAD v4: 10-62528651-A-AG
• MyVariant Identifiers: chr10:g.64288410_64288411insG (hg19) ; chr10:g.62528651_62528652insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62528651_62528652insG , CM000672.2:g.62528651_62528652insG	GRCh38
NC_000010.10:g.64288410_64288411insG , CM000672.1:g.64288410_64288411insG	GRCh37
NC_000010.9:g.63958416_63958417insG	NCBI36
NG_021209.1:g.159495_159496insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+68854_981+68855insG	ENSP00000502188.1:n.981+68854_981+68855insG
ENST00000395251.5:c.-185+8054_-185+8055insG	ENSP00000378672.1:n.-185+8054_-185+8055insG
ENST00000410046.7:c.981+68854_981+68855insG	ENSP00000387091.3:n.981+68854_981+68855insG
NM_199451.2:c.981+68854_981+68855insG	NP_955523.1:n.981+68854_981+68855insG
NM_199452.3:c.-185+8054_-185+8055insG	NP_955524.3:n.-185+8054_-185+8055insG
XM_017015937.2:c.982-15558_982-15557insG	XP_016871426.1:n.982-15558_982-15557insG
NM_199451.3:c.981+68854_981+68855insG	NP_955523.1:n.981+68854_981+68855insG