Canonical Allele Identifier: CA1499157095

Gene: ZNF330

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221491_141221499delinsTTGGCCAGG , CM000666.2:g.141221491_141221499delinsTTGGCCAGG	GRCh38
NC_000004.11:g.142142645_142142653delinsTTGGCCAGG , CM000666.1:g.142142645_142142653delinsTTGGCCAGG	GRCh37
NC_000004.10:g.142362095_142362103delinsTTGGCCAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+383_-7+391delinsTTGGCCAGG MANE Select	ENSP00000262990.4:n.-7+383_-7+391delinsTTGGCCAGG
ENST00000262990.8:c.-7+383_-7+391delinsTTGGCCAGG	ENSP00000262990.4:n.-7+383_-7+391delinsTTGGCCAGG
ENST00000503649.5:c.-7+414_-7+422delinsTTGGCCAGG	ENSP00000422966.1:n.-7+414_-7+422delinsTTGGCCAGG
ENST00000506302.1:c.-7+383_-7+391delinsTTGGCCAGG	ENSP00000427201.1:n.-7+383_-7+391delinsTTGGCCAGG
ENST00000507532.5:c.-7+383_-7+391delinsTTGGCCAGG	ENSP00000422574.1:n.-7+383_-7+391delinsTTGGCCAGG
ENST00000512738.5:c.-7+475_-7+483delinsTTGGCCAGG	ENSP00000422251.1:n.-7+475_-7+483delinsTTGGCCAGG
ENST00000512809.5:c.-7+437_-7+445delinsTTGGCCAGG	ENSP00000422599.1:n.-7+437_-7+445delinsTTGGCCAGG
ENST00000514826.5:n.222+383_222+391delinsTTGGCCAGG
ENST00000515453.5:c.-7+383_-7+391delinsTTGGCCAGG	ENSP00000423217.1:n.-7+383_-7+391delinsTTGGCCAGG
NM_001292002.1:c.-116+383_-116+391delinsTTGGCCAGG	NP_001278931.1:n.-116+383_-116+391delinsTTGGCCAGG
NM_014487.5:c.-7+383_-7+391delinsTTGGCCAGG	NP_055302.1:n.-7+383_-7+391delinsTTGGCCAGG
XM_011531875.1:c.-6-875_-6-867delinsTTGGCCAGG	XP_011530177.1:n.-6-875_-6-867delinsTTGGCCAGG
XM_017008033.1:c.-7+832_-7+840delinsTTGGCCAGG	XP_016863522.1:n.-7+832_-7+840delinsTTGGCCAGG
XM_024453986.1:c.-7+414_-7+422delinsTTGGCCAGG	XP_024309754.1:n.-7+414_-7+422delinsTTGGCCAGG
NM_014487.6:c.-7+383_-7+391delinsTTGGCCAGG MANE Select	NP_055302.1:n.-7+383_-7+391delinsTTGGCCAGG
NM_001292002.2:c.-116+383_-116+391delinsTTGGCCAGG	NP_001278931.1:n.-116+383_-116+391delinsTTGGCCAGG