Canonical Allele Identifier: CA667276668

Gene: ZNF365

Linked Data

• dbSNP Id: rs1390070231
• gnomAD v3: 10-62531279-A-AAGCAAGTG
• gnomAD v4: 10-62531279-A-AAGCAAGTG
• MyVariant Identifiers: chr10:g.64291038_64291039insAGCAAGTG (hg19) ; chr10:g.62531279_62531280insAGCAAGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531281_62531288dup , CM000672.2:g.62531281_62531288dup	GRCh38
NC_000010.10:g.64291040_64291047dup , CM000672.1:g.64291040_64291047dup	GRCh37
NC_000010.9:g.63961046_63961053dup	NCBI36
NG_021209.1:g.162125_162132dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71484_981+71491dup	ENSP00000502188.1:n.981+71484_981+71491dup
ENST00000395251.5:c.-185+10684_-185+10691dup	ENSP00000378672.1:n.-185+10684_-185+10691dup
ENST00000410046.7:c.981+71484_981+71491dup	ENSP00000387091.3:n.981+71484_981+71491dup
NM_199451.2:c.981+71484_981+71491dup	NP_955523.1:n.981+71484_981+71491dup
NM_199452.3:c.-185+10684_-185+10691dup	NP_955524.3:n.-185+10684_-185+10691dup
XM_017015937.2:c.982-12928_982-12921dup	XP_016871426.1:n.982-12928_982-12921dup
NM_199451.3:c.981+71484_981+71491dup	NP_955523.1:n.981+71484_981+71491dup