Canonical Allele Identifier: CA1068796608

Gene: ZNF330

Linked Data

• gnomAD v3: 4-141221612-A-T
• gnomAD v4: 4-141221612-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221612A>T , CM000666.2:g.141221612A>T	GRCh38
NC_000004.11:g.142142766A>T , CM000666.1:g.142142766A>T	GRCh37
NC_000004.10:g.142362216A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+504A>T MANE Select	ENSP00000262990.4:n.-7+504A>T
ENST00000262990.8:c.-7+504A>T	ENSP00000262990.4:n.-7+504A>T
ENST00000503649.5:c.-7+535A>T	ENSP00000422966.1:n.-7+535A>T
ENST00000506302.1:c.-7+504A>T	ENSP00000427201.1:n.-7+504A>T
ENST00000507532.5:c.-7+504A>T	ENSP00000422574.1:n.-7+504A>T
ENST00000512738.5:c.-7+596A>T	ENSP00000422251.1:n.-7+596A>T
ENST00000512809.5:c.-7+558A>T	ENSP00000422599.1:n.-7+558A>T
ENST00000514826.5:n.222+504A>T
ENST00000515453.5:c.-7+504A>T	ENSP00000423217.1:n.-7+504A>T
NM_001292002.1:c.-116+504A>T	NP_001278931.1:n.-116+504A>T
NM_014487.5:c.-7+504A>T	NP_055302.1:n.-7+504A>T
XM_011531875.1:c.-6-754A>T	XP_011530177.1:n.-6-754A>T
XM_017008033.1:c.-6-754A>T	XP_016863522.1:n.-6-754A>T
XM_024453986.1:c.-7+535A>T	XP_024309754.1:n.-7+535A>T
NM_014487.6:c.-7+504A>T MANE Select	NP_055302.1:n.-7+504A>T
NM_001292002.2:c.-116+504A>T	NP_001278931.1:n.-116+504A>T