Canonical Allele Identifier: CA1499157152

Gene: ZNF330

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221554T= , CM000666.2:g.141221554T=	GRCh38
NC_000004.11:g.142142708T= , CM000666.1:g.142142708T=	GRCh37
NC_000004.10:g.142362158T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262990.9:c.-7+446T= MANE Select	ENSP00000262990.4:n.-7+446T=
ENST00000262990.8:c.-7+446T=	ENSP00000262990.4:n.-7+446T=
ENST00000503649.5:c.-7+477T=	ENSP00000422966.1:n.-7+477T=
ENST00000506302.1:c.-7+446T=	ENSP00000427201.1:n.-7+446T=
ENST00000507532.5:c.-7+446T=	ENSP00000422574.1:n.-7+446T=
ENST00000512738.5:c.-7+538T=	ENSP00000422251.1:n.-7+538T=
ENST00000512809.5:c.-7+500T=	ENSP00000422599.1:n.-7+500T=
ENST00000514826.5:n.222+446T=
ENST00000515453.5:c.-7+446T=	ENSP00000423217.1:n.-7+446T=
NM_001292002.1:c.-116+446T=	NP_001278931.1:n.-116+446T=
NM_014487.5:c.-7+446T=	NP_055302.1:n.-7+446T=
XM_011531875.1:c.-6-812T=	XP_011530177.1:n.-6-812T=
XM_017008033.1:c.-6-812T=	XP_016863522.1:n.-6-812T=
XM_024453986.1:c.-7+477T=	XP_024309754.1:n.-7+477T=
NM_014487.6:c.-7+446T= MANE Select	NP_055302.1:n.-7+446T=
NM_001292002.2:c.-116+446T=	NP_001278931.1:n.-116+446T=