Canonical Allele Identifier: CA667277168

Gene: ZNF365

Linked Data

• dbSNP Id: rs1242277133
• MyVariant Identifiers: chr10:g.64291441_64291442insGG (hg19) ; chr10:g.62531682_62531683insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531682_62531683insGG , CM000672.2:g.62531682_62531683insGG	GRCh38
NC_000010.10:g.64291441_64291442insGG , CM000672.1:g.64291441_64291442insGG	GRCh37
NC_000010.9:g.63961447_63961448insGG	NCBI36
NG_021209.1:g.162526_162527insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71885_981+71886insGG	ENSP00000502188.1:n.981+71885_981+71886insGG
ENST00000395251.5:c.-185+11085_-185+11086insGG	ENSP00000378672.1:n.-185+11085_-185+11086insGG
ENST00000410046.7:c.981+71885_981+71886insGG	ENSP00000387091.3:n.981+71885_981+71886insGG
NM_199451.2:c.981+71885_981+71886insGG	NP_955523.1:n.981+71885_981+71886insGG
NM_199452.3:c.-185+11085_-185+11086insGG	NP_955524.3:n.-185+11085_-185+11086insGG
XM_017015937.2:c.982-12527_982-12526insGG	XP_016871426.1:n.982-12527_982-12526insGG
NM_199451.3:c.981+71885_981+71886insGG	NP_955523.1:n.981+71885_981+71886insGG