Canonical Allele Identifier: CA1499157109

Gene: ZNF330

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141221510C= , CM000666.2:g.141221510C=	GRCh38
NC_000004.11:g.142142664C= , CM000666.1:g.142142664C=	GRCh37
NC_000004.10:g.142362114C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262990.9:c.-7+402C= MANE Select	ENSP00000262990.4:n.-7+402C=
ENST00000262990.8:c.-7+402C=	ENSP00000262990.4:n.-7+402C=
ENST00000503649.5:c.-7+433C=	ENSP00000422966.1:n.-7+433C=
ENST00000506302.1:c.-7+402C=	ENSP00000427201.1:n.-7+402C=
ENST00000507532.5:c.-7+402C=	ENSP00000422574.1:n.-7+402C=
ENST00000512738.5:c.-7+494C=	ENSP00000422251.1:n.-7+494C=
ENST00000512809.5:c.-7+456C=	ENSP00000422599.1:n.-7+456C=
ENST00000514826.5:n.222+402C=
ENST00000515453.5:c.-7+402C=	ENSP00000423217.1:n.-7+402C=
NM_001292002.1:c.-116+402C=	NP_001278931.1:n.-116+402C=
NM_014487.5:c.-7+402C=	NP_055302.1:n.-7+402C=
XM_011531875.1:c.-6-856C=	XP_011530177.1:n.-6-856C=
XM_017008033.1:c.-7+851C=	XP_016863522.1:n.-7+851C=
XM_024453986.1:c.-7+433C=	XP_024309754.1:n.-7+433C=
NM_014487.6:c.-7+402C= MANE Select	NP_055302.1:n.-7+402C=
NM_001292002.2:c.-116+402C=	NP_001278931.1:n.-116+402C=