Canonical Allele Identifier: CA594035787

Gene: ZNF365

Linked Data

• dbSNP Id: rs1564623819
• gnomAD v2: 10-64291078-G-GGT
• gnomAD v3: 10-62531319-G-GGT
• gnomAD v4: 10-62531319-G-GGT
• MyVariant Identifiers: chr10:g.64291080delinsTGC (hg19) ; chr10:g.62531321delinsTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531320_62531321insTG , CM000672.2:g.62531320_62531321insTG	GRCh38
NC_000010.10:g.64291079_64291080insTG , CM000672.1:g.64291079_64291080insTG	GRCh37
NC_000010.9:g.63961085_63961086insTG	NCBI36
NG_021209.1:g.162164_162165insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71523_981+71524insTG	ENSP00000502188.1:n.981+71523_981+71524insTG
ENST00000395251.5:c.-185+10723_-185+10724insTG	ENSP00000378672.1:n.-185+10723_-185+10724insTG
ENST00000410046.7:c.981+71523_981+71524insTG	ENSP00000387091.3:n.981+71523_981+71524insTG
NM_199451.2:c.981+71523_981+71524insTG	NP_955523.1:n.981+71523_981+71524insTG
NM_199452.3:c.-185+10723_-185+10724insTG	NP_955524.3:n.-185+10723_-185+10724insTG
XM_017015937.2:c.982-12889_982-12888insTG	XP_016871426.1:n.982-12889_982-12888insTG
NM_199451.3:c.981+71523_981+71524insTG	NP_955523.1:n.981+71523_981+71524insTG