Canonical Allele Identifier: CA1499157096

Gene: ZNF330

Linked Data

• dbSNP Id: rs1728676348

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221492_141221499del , CM000666.2:g.141221492_141221499del	GRCh38
NC_000004.11:g.142142646_142142653del , CM000666.1:g.142142646_142142653del	GRCh37
NC_000004.10:g.142362096_142362103del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+384_-7+391del MANE Select	ENSP00000262990.4:n.-7+384_-7+391del
ENST00000262990.8:c.-7+384_-7+391del	ENSP00000262990.4:n.-7+384_-7+391del
ENST00000503649.5:c.-7+415_-7+422del	ENSP00000422966.1:n.-7+415_-7+422del
ENST00000506302.1:c.-7+384_-7+391del	ENSP00000427201.1:n.-7+384_-7+391del
ENST00000507532.5:c.-7+384_-7+391del	ENSP00000422574.1:n.-7+384_-7+391del
ENST00000512738.5:c.-7+476_-7+483del	ENSP00000422251.1:n.-7+476_-7+483del
ENST00000512809.5:c.-7+438_-7+445del	ENSP00000422599.1:n.-7+438_-7+445del
ENST00000514826.5:n.222+384_222+391del
ENST00000515453.5:c.-7+384_-7+391del	ENSP00000423217.1:n.-7+384_-7+391del
NM_001292002.1:c.-116+384_-116+391del	NP_001278931.1:n.-116+384_-116+391del
NM_014487.5:c.-7+384_-7+391del	NP_055302.1:n.-7+384_-7+391del
XM_011531875.1:c.-6-874_-6-867del	XP_011530177.1:n.-6-874_-6-867del
XM_017008033.1:c.-7+833_-7+840del	XP_016863522.1:n.-7+833_-7+840del
XM_024453986.1:c.-7+415_-7+422del	XP_024309754.1:n.-7+415_-7+422del
NM_014487.6:c.-7+384_-7+391del MANE Select	NP_055302.1:n.-7+384_-7+391del
NM_001292002.2:c.-116+384_-116+391del	NP_001278931.1:n.-116+384_-116+391del