Canonical Allele Identifier: CA1499157122

Gene: ZNF330

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221524_141221525delinsAT , CM000666.2:g.141221524_141221525delinsAT	GRCh38
NC_000004.11:g.142142678_142142679delinsAT , CM000666.1:g.142142678_142142679delinsAT	GRCh37
NC_000004.10:g.142362128_142362129delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+416_-7+417delinsAT MANE Select	ENSP00000262990.4:n.-7+416_-7+417delinsAT
ENST00000262990.8:c.-7+416_-7+417delinsAT	ENSP00000262990.4:n.-7+416_-7+417delinsAT
ENST00000503649.5:c.-7+447_-7+448delinsAT	ENSP00000422966.1:n.-7+447_-7+448delinsAT
ENST00000506302.1:c.-7+416_-7+417delinsAT	ENSP00000427201.1:n.-7+416_-7+417delinsAT
ENST00000507532.5:c.-7+416_-7+417delinsAT	ENSP00000422574.1:n.-7+416_-7+417delinsAT
ENST00000512738.5:c.-7+508_-7+509delinsAT	ENSP00000422251.1:n.-7+508_-7+509delinsAT
ENST00000512809.5:c.-7+470_-7+471delinsAT	ENSP00000422599.1:n.-7+470_-7+471delinsAT
ENST00000514826.5:n.222+416_222+417delinsAT
ENST00000515453.5:c.-7+416_-7+417delinsAT	ENSP00000423217.1:n.-7+416_-7+417delinsAT
NM_001292002.1:c.-116+416_-116+417delinsAT	NP_001278931.1:n.-116+416_-116+417delinsAT
NM_014487.5:c.-7+416_-7+417delinsAT	NP_055302.1:n.-7+416_-7+417delinsAT
XM_011531875.1:c.-6-842_-6-841delinsAT	XP_011530177.1:n.-6-842_-6-841delinsAT
XM_017008033.1:c.-6-842_-6-841delinsAT	XP_016863522.1:n.-6-842_-6-841delinsAT
XM_024453986.1:c.-7+447_-7+448delinsAT	XP_024309754.1:n.-7+447_-7+448delinsAT
NM_014487.6:c.-7+416_-7+417delinsAT MANE Select	NP_055302.1:n.-7+416_-7+417delinsAT
NM_001292002.2:c.-116+416_-116+417delinsAT	NP_001278931.1:n.-116+416_-116+417delinsAT