Canonical Allele Identifier: CA745561573

Gene: ZNF217 ZNF217-AS1

Linked Data

• dbSNP Id: rs1259068616
• MyVariant Identifiers: chr20:g.52183606_52183607insG (hg19) ; chr20:g.53567067_53567068insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.53567067_53567068insG , CM000682.2:g.53567067_53567068insG	GRCh38
NC_000020.10:g.52183606_52183607insG , CM000682.1:g.52183606_52183607insG	GRCh37
NC_000020.9:g.51617013_51617014insG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371471.6:c.*2220_*2221insC (ZNF217)	ENSP00000360526.2:n.*2220_*2221insC
NR_110051.1:n.556-3205_556-3204insG (ZNF217-AS1)
XM_005260545.2:c.*2048_*2049insC (ZNF217)	XP_005260602.1:n.*2048_*2049insC
XM_006723875.2:c.*2048_*2049insC (ZNF217)	XP_006723938.1:n.*2048_*2049insC
XM_011529036.1:c.*2048_*2049insC (ZNF217)	XP_011527338.1:n.*2048_*2049insC
XM_005260545.4:c.*2048_*2049insC (ZNF217)	XP_005260602.1:n.*2048_*2049insC
XM_024451996.1:c.*2048_*2049insC (ZNF217)	XP_024307764.1:n.*2048_*2049insC
XM_024451997.1:c.*2048_*2049insC (ZNF217)	XP_024307765.1:n.*2048_*2049insC
XM_024451998.1:c.*2048_*2049insC (ZNF217)	XP_024307766.1:n.*2048_*2049insC