Canonical Allele Identifier: CA2203508488

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762572_4762574delinsCCT , CM000678.2:g.4762572_4762574delinsCCT	GRCh38
NC_000016.9:g.4812573_4812575delinsCCT , CM000678.1:g.4812573_4812575delinsCCT	GRCh37
NC_000016.8:g.4752574_4752576delinsCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.597_598+1delinsAGG
ENST00000219478.10:c.597_598+1delinsAGG
ENST00000545009.1:c.597_598+1delinsAGG
ENST00000589422.1:c.*125_*126+1delinsAGG
NM_001303450.1:c.597_598+1delinsAGG
NM_021646.2:c.597_598+1delinsAGG
XM_005255243.2:c.246_247+1delinsAGG
XM_011522453.1:c.597_598+1delinsAGG
XM_011522454.1:c.-28_-27+1delinsAGG
NM_021646.3:c.597_598+1delinsAGG
XM_005255243.4:c.246_247+1delinsAGG
XM_011522453.2:c.597_598+1delinsAGG
XM_011522454.3:c.-28_-27+1delinsAGG
XM_017023121.2:c.-28_-27+1delinsAGG
NM_001303450.2:c.597_598+1delinsAGG
NM_021646.4:c.597_598+1delinsAGG