Canonical Allele Identifier: CA594035209

Gene: ZNF365

Linked Data

• gnomAD v2: 10-64288395-C-CA
• gnomAD v3: 10-62528636-C-CA
• gnomAD v4: 10-62528636-C-CA
• MyVariant Identifiers: chr10:g.64288395_64288396insA (hg19) ; chr10:g.62528636_62528637insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62528637dup , CM000672.2:g.62528637dup	GRCh38
NC_000010.10:g.64288396dup , CM000672.1:g.64288396dup	GRCh37
NC_000010.9:g.63958402dup	NCBI36
NG_021209.1:g.159481dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+68840dup	ENSP00000502188.1:n.981+68840dup
ENST00000395251.5:c.-185+8040dup	ENSP00000378672.1:n.-185+8040dup
ENST00000410046.7:c.981+68840dup	ENSP00000387091.3:n.981+68840dup
NM_199451.2:c.981+68840dup	NP_955523.1:n.981+68840dup
NM_199452.3:c.-185+8040dup	NP_955524.3:n.-185+8040dup
XM_017015937.2:c.982-15572dup	XP_016871426.1:n.982-15572dup
NM_199451.3:c.981+68840dup	NP_955523.1:n.981+68840dup