Canonical Allele Identifier: CA594035823

Gene: ZNF365

Linked Data

• dbSNP Id: rs1347393118
• gnomAD v2: 10-64291353-T-TAAAA
• gnomAD v3: 10-62531594-T-TAAAA
• gnomAD v4: 10-62531594-T-TAAAA
• MyVariant Identifiers: chr10:g.64291353_64291354insAAAA (hg19) ; chr10:g.62531594_62531595insAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531594_62531595insAAAA , CM000672.2:g.62531594_62531595insAAAA	GRCh38
NC_000010.10:g.64291353_64291354insAAAA , CM000672.1:g.64291353_64291354insAAAA	GRCh37
NC_000010.9:g.63961359_63961360insAAAA	NCBI36
NG_021209.1:g.162438_162439insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71797_981+71798insAAAA	ENSP00000502188.1:n.981+71797_981+71798insAAAA
ENST00000395251.5:c.-185+10997_-185+10998insAAAA	ENSP00000378672.1:n.-185+10997_-185+10998insAAAA
ENST00000410046.7:c.981+71797_981+71798insAAAA	ENSP00000387091.3:n.981+71797_981+71798insAAAA
NM_199451.2:c.981+71797_981+71798insAAAA	NP_955523.1:n.981+71797_981+71798insAAAA
NM_199452.3:c.-185+10997_-185+10998insAAAA	NP_955524.3:n.-185+10997_-185+10998insAAAA
XM_017015937.2:c.982-12615_982-12614insAAAA	XP_016871426.1:n.982-12615_982-12614insAAAA
NM_199451.3:c.981+71797_981+71798insAAAA	NP_955523.1:n.981+71797_981+71798insAAAA