Canonical Allele Identifier: CA667276869

Gene: ZNF365

Linked Data

• dbSNP Id: rs1331909380
• MyVariant Identifiers: chr10:g.64291221_64291239del (hg19) ; chr10:g.62531462_62531480del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62531466_62531484del , CM000672.2:g.62531466_62531484del	GRCh38
NC_000010.10:g.64291225_64291243del , CM000672.1:g.64291225_64291243del	GRCh37
NC_000010.9:g.63961231_63961249del	NCBI36
NG_021209.1:g.162310_162328del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647733.1:c.981+71669_981+71687del	ENSP00000502188.1:n.981+71669_981+71687del
ENST00000395251.5:c.-185+10869_-185+10887del	ENSP00000378672.1:n.-185+10869_-185+10887del
ENST00000410046.7:c.981+71669_981+71687del	ENSP00000387091.3:n.981+71669_981+71687del
NM_199451.2:c.981+71669_981+71687del	NP_955523.1:n.981+71669_981+71687del
NM_199452.3:c.-185+10869_-185+10887del	NP_955524.3:n.-185+10869_-185+10887del
XM_017015937.2:c.982-12743_982-12725del	XP_016871426.1:n.982-12743_982-12725del
NM_199451.3:c.981+71669_981+71687del	NP_955523.1:n.981+71669_981+71687del