Canonical Allele Identifier: CA555070858

Gene: ZNF330

Linked Data

• dbSNP Id: rs1431385578
• gnomAD v2: 4-142142678-AT-A
• gnomAD v3: 4-141221524-AT-A
• gnomAD v4: 4-141221524-AT-A
• MyVariant Identifiers: chr4:g.142142679del (hg19) ; chr4:g.141221525del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221528del , CM000666.2:g.141221528del	GRCh38
NC_000004.11:g.142142682del , CM000666.1:g.142142682del	GRCh37
NC_000004.10:g.142362132del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+420del MANE Select	ENSP00000262990.4:n.-7+420del
ENST00000262990.8:c.-7+420del	ENSP00000262990.4:n.-7+420del
ENST00000503649.5:c.-7+451del	ENSP00000422966.1:n.-7+451del
ENST00000506302.1:c.-7+420del	ENSP00000427201.1:n.-7+420del
ENST00000507532.5:c.-7+420del	ENSP00000422574.1:n.-7+420del
ENST00000512738.5:c.-7+512del	ENSP00000422251.1:n.-7+512del
ENST00000512809.5:c.-7+474del	ENSP00000422599.1:n.-7+474del
ENST00000514826.5:n.222+420del
ENST00000515453.5:c.-7+420del	ENSP00000423217.1:n.-7+420del
NM_001292002.1:c.-116+420del	NP_001278931.1:n.-116+420del
NM_014487.5:c.-7+420del	NP_055302.1:n.-7+420del
XM_011531875.1:c.-6-838del	XP_011530177.1:n.-6-838del
XM_017008033.1:c.-6-838del	XP_016863522.1:n.-6-838del
XM_024453986.1:c.-7+451del	XP_024309754.1:n.-7+451del
NM_014487.6:c.-7+420del MANE Select	NP_055302.1:n.-7+420del
NM_001292002.2:c.-116+420del	NP_001278931.1:n.-116+420del