Canonical Allele Identifier: CA667276870

Gene: ZNF365

Linked Data

• dbSNP Id: rs1409330754
• MyVariant Identifiers: chr10:g.64291225_64291226insTGCACCT (hg19) ; chr10:g.62531466_62531467insTGCACCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531467_62531473dup , CM000672.2:g.62531467_62531473dup	GRCh38
NC_000010.10:g.64291226_64291232dup , CM000672.1:g.64291226_64291232dup	GRCh37
NC_000010.9:g.63961232_63961238dup	NCBI36
NG_021209.1:g.162311_162317dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647733.1:c.981+71670_981+71676dup	ENSP00000502188.1:n.981+71670_981+71676dup
ENST00000395251.5:c.-185+10870_-185+10876dup	ENSP00000378672.1:n.-185+10870_-185+10876dup
ENST00000410046.7:c.981+71670_981+71676dup	ENSP00000387091.3:n.981+71670_981+71676dup
NM_199451.2:c.981+71670_981+71676dup	NP_955523.1:n.981+71670_981+71676dup
NM_199452.3:c.-185+10870_-185+10876dup	NP_955524.3:n.-185+10870_-185+10876dup
XM_017015937.2:c.982-12742_982-12736dup	XP_016871426.1:n.982-12742_982-12736dup
NM_199451.3:c.981+71670_981+71676dup	NP_955523.1:n.981+71670_981+71676dup