Canonical Allele Identifier: CA1499157014

Gene: ZNF330

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221394_141221397delinsAAAT , CM000666.2:g.141221394_141221397delinsAAAT	GRCh38
NC_000004.11:g.142142548_142142551delinsAAAT , CM000666.1:g.142142548_142142551delinsAAAT	GRCh37
NC_000004.10:g.142361998_142362001delinsAAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262990.9:c.-7+286_-7+289delinsAAAT MANE Select	ENSP00000262990.4:n.-7+286_-7+289delinsAAAT
ENST00000262990.8:c.-7+286_-7+289delinsAAAT	ENSP00000262990.4:n.-7+286_-7+289delinsAAAT
ENST00000503649.5:c.-7+317_-7+320delinsAAAT	ENSP00000422966.1:n.-7+317_-7+320delinsAAAT
ENST00000506302.1:c.-7+286_-7+289delinsAAAT	ENSP00000427201.1:n.-7+286_-7+289delinsAAAT
ENST00000507532.5:c.-7+286_-7+289delinsAAAT	ENSP00000422574.1:n.-7+286_-7+289delinsAAAT
ENST00000512738.5:c.-7+378_-7+381delinsAAAT	ENSP00000422251.1:n.-7+378_-7+381delinsAAAT
ENST00000512809.5:c.-7+340_-7+343delinsAAAT	ENSP00000422599.1:n.-7+340_-7+343delinsAAAT
ENST00000514826.5:n.222+286_222+289delinsAAAT
ENST00000515453.5:c.-7+286_-7+289delinsAAAT	ENSP00000423217.1:n.-7+286_-7+289delinsAAAT
NM_001292002.1:c.-116+286_-116+289delinsAAAT	NP_001278931.1:n.-116+286_-116+289delinsAAAT
NM_014487.5:c.-7+286_-7+289delinsAAAT	NP_055302.1:n.-7+286_-7+289delinsAAAT
XM_011531875.1:c.-7+834_-7+837delinsAAAT	XP_011530177.1:n.-7+834_-7+837delinsAAAT
XM_017008033.1:c.-7+735_-7+738delinsAAAT	XP_016863522.1:n.-7+735_-7+738delinsAAAT
XM_024453986.1:c.-7+317_-7+320delinsAAAT	XP_024309754.1:n.-7+317_-7+320delinsAAAT
NM_014487.6:c.-7+286_-7+289delinsAAAT MANE Select	NP_055302.1:n.-7+286_-7+289delinsAAAT
NM_001292002.2:c.-116+286_-116+289delinsAAAT	NP_001278931.1:n.-116+286_-116+289delinsAAAT