Canonical Allele Identifier: CA316149397

Gene: ZNF217 ZNF217-AS1

Linked Data

• dbSNP Id: rs369079322
• gnomAD v2: 20-52183611-TGCAAA-T
• gnomAD v3: 20-53567072-TGCAAA-T
• gnomAD v4: 20-53567072-TGCAAA-T
• MyVariant Identifiers: chr20:g.52183612_52183616del (hg19) ; chr20:g.53567073_53567077del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.53567073_53567077del , CM000682.2:g.53567073_53567077del	GRCh38
NC_000020.10:g.52183612_52183616del , CM000682.1:g.52183612_52183616del	GRCh37
NC_000020.9:g.51617019_51617023del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371471.7:c.*2211_*2215del (ZNF217) MANE Select	ENSP00000360526.2:n.*2211_*2215del
ENST00000302342.3:c.*2211_*2215del (ZNF217)	ENSP00000304308.3:n.*2211_*2215del
ENST00000371471.6:c.*2211_*2215del (ZNF217)	ENSP00000360526.2:n.*2211_*2215del
NM_006526.2:c.*2211_*2215del (ZNF217)	NP_006517.1:n.*2211_*2215del
NR_110051.1:n.556-3199_556-3195del (ZNF217-AS1)
XM_005260545.2:c.*2039_*2043del (ZNF217)	XP_005260602.1:n.*2039_*2043del
XM_006723875.2:c.*2039_*2043del (ZNF217)	XP_006723938.1:n.*2039_*2043del
XM_011529036.1:c.*2039_*2043del (ZNF217)	XP_011527338.1:n.*2039_*2043del
XM_005260545.4:c.*2039_*2043del (ZNF217)	XP_005260602.1:n.*2039_*2043del
XM_017028059.2:c.*2211_*2215del (ZNF217)	XP_016883548.1:n.*2211_*2215del
XM_024451996.1:c.*2039_*2043del (ZNF217)	XP_024307764.1:n.*2039_*2043del
XM_024451997.1:c.*2039_*2043del (ZNF217)	XP_024307765.1:n.*2039_*2043del
XM_024451998.1:c.*2039_*2043del (ZNF217)	XP_024307766.1:n.*2039_*2043del
NM_001385034.1:c.*2039_*2043del (ZNF217)	NP_001371963.1:n.*2039_*2043del
NM_006526.3:c.*2211_*2215del (ZNF217) MANE Select	NP_006517.1:n.*2211_*2215del