Canonical Allele Identifier: CA594035786

Gene: ZNF365

Linked Data

• dbSNP Id: rs1267954752
• gnomAD v2: 10-64291078-GGC-G
• gnomAD v3: 10-62531319-GGC-G
• gnomAD v4: 10-62531319-GGC-G
• MyVariant Identifiers: chr10:g.64291079_64291080del (hg19) ; chr10:g.62531320_62531321del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531322_62531323del , CM000672.2:g.62531322_62531323del	GRCh38
NC_000010.10:g.64291081_64291082del , CM000672.1:g.64291081_64291082del	GRCh37
NC_000010.9:g.63961087_63961088del	NCBI36
NG_021209.1:g.162166_162167del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71525_981+71526del	ENSP00000502188.1:n.981+71525_981+71526del
ENST00000395251.5:c.-185+10725_-185+10726del	ENSP00000378672.1:n.-185+10725_-185+10726del
ENST00000410046.7:c.981+71525_981+71526del	ENSP00000387091.3:n.981+71525_981+71526del
NM_199451.2:c.981+71525_981+71526del	NP_955523.1:n.981+71525_981+71526del
NM_199452.3:c.-185+10725_-185+10726del	NP_955524.3:n.-185+10725_-185+10726del
XM_017015937.2:c.982-12887_982-12886del	XP_016871426.1:n.982-12887_982-12886del
NM_199451.3:c.981+71525_981+71526del	NP_955523.1:n.981+71525_981+71526del