Canonical Allele Identifier: CA390566377

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077267G>C (hg19) ; chr14:g.88610923G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610923G>C , CM000676.2:g.88610923G>C	GRCh38
NC_000014.8:g.89077267G>C , CM000676.1:g.89077267G>C	GRCh37
NC_000014.7:g.88147020G>C	NCBI36
NG_050601.1:g.53015G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2187G>C MANE Select	ENSP00000251038.5:p.Trp729Cys
ENST00000649731.1:c.*1395G>C	ENSP00000497757.1:n.*1395G>C
ENST00000251038.9:c.2187G>C	ENSP00000251038.5:p.Trp729Cys
ENST00000302216.12:c.1716G>C	ENSP00000307025.8:p.Trp572Cys
ENST00000318308.10:c.897G>C	ENSP00000327176.6:p.Trp299Cys
ENST00000336693.8:c.1692G>C	ENSP00000338002.4:p.Trp564Cys
ENST00000393514.9:c.2112G>C	ENSP00000377150.5:p.Trp704Cys
ENST00000406216.7:c.825G>C	ENSP00000384682.3:p.Trp275Cys
ENST00000554020.5:n.1030G>C
ENST00000555755.5:c.2169G>C	ENSP00000452475.1:p.Trp723Cys
ENST00000555792.1:c.432G>C	ENSP00000450823.1:p.Trp144Cys
ENST00000555851.6:n.346G>C
ENST00000555900.5:c.1293G>C	ENSP00000451530.1:p.Trp431Cys
ENST00000556000.5:c.1931G>C
ENST00000556945.5:c.1794G>C	ENSP00000450474.1:p.Trp598Cys
ENST00000557491.1:n.1472G>C
ENST00000557607.5:c.1239G>C	ENSP00000452370.1:p.Trp413Cys
NM_001160103.1:c.2184G>C	NP_001153575.1:p.Trp728Cys
NM_001160104.1:c.2169G>C	NP_001153576.1:p.Trp723Cys
NM_024824.4:c.2187G>C	NP_079100.2:p.Trp729Cys
NM_207660.3:c.1716G>C	NP_997543.1:p.Trp572Cys
NM_207661.2:c.1692G>C	NP_997544.1:p.Trp564Cys
NM_207662.3:c.897G>C	NP_997545.2:p.Trp299Cys
XM_005268067.3:c.2172G>C	XP_005268124.1:p.Trp724Cys
XM_005268068.3:c.2112G>C	XP_005268125.1:p.Trp704Cys
XM_005268069.3:c.1794G>C	XP_005268126.1:p.Trp598Cys
XM_005268070.3:c.1791G>C	XP_005268127.1:p.Trp597Cys
XM_005268071.3:c.1719G>C	XP_005268128.1:p.Trp573Cys
XM_005268073.3:c.1293G>C	XP_005268130.1:p.Trp431Cys
XM_006720257.2:c.1218G>C	XP_006720320.1:p.Trp406Cys
XM_011537160.1:c.2085G>C	XP_011535462.1:p.Trp695Cys
XM_011537161.1:c.2031G>C	XP_011535463.1:p.Trp677Cys
NM_001326295.1:c.1794G>C	NP_001313224.1:p.Trp598Cys
NM_001326296.1:c.2109G>C	NP_001313225.1:p.Trp703Cys
NM_001326297.1:c.2085G>C	NP_001313226.1:p.Trp695Cys
NM_001326298.1:c.1719G>C	NP_001313227.1:p.Trp573Cys
NM_001326299.1:c.2094G>C	NP_001313228.1:p.Trp698Cys
NM_001326300.1:c.1722G>C	NP_001313229.1:p.Trp574Cys
NM_001326301.1:c.2010G>C	NP_001313230.1:p.Trp670Cys
NM_001326302.1:c.1719G>C	NP_001313231.1:p.Trp573Cys
NM_001326303.1:c.1614G>C	NP_001313232.1:p.Trp538Cys
NM_001326304.1:c.1326G>C	NP_001313233.1:p.Trp442Cys
NM_001326305.1:c.1647G>C	NP_001313234.1:p.Trp549Cys
NM_001326306.1:c.1560G>C	NP_001313235.1:p.Trp520Cys
NM_001326307.1:c.2112G>C	NP_001313236.1:p.Trp704Cys
NM_001326308.1:c.1329G>C	NP_001313237.1:p.Trp443Cys
NM_001326309.1:c.1254G>C	NP_001313238.1:p.Trp418Cys
NM_001326310.1:c.2172G>C	NP_001313239.1:p.Trp724Cys
NM_001326311.1:c.1251G>C	NP_001313240.1:p.Trp417Cys
NM_001326312.1:c.2097G>C	NP_001313241.1:p.Trp699Cys
NM_001326313.1:c.1563G>C	NP_001313242.1:p.Trp521Cys
NM_001326314.1:c.1644G>C	NP_001313243.1:p.Trp548Cys
NM_001326315.1:c.2082G>C	NP_001313244.1:p.Trp694Cys
NM_001326316.1:c.2082G>C	NP_001313245.1:p.Trp694Cys
NR_136936.1:n.2252G>C
XM_005268070.5:c.1791G>C	XP_005268127.1:p.Trp597Cys
XM_005268073.4:c.1293G>C	XP_005268130.1:p.Trp431Cys
XM_006720257.3:c.1218G>C	XP_006720320.1:p.Trp406Cys
XM_011537161.3:c.2031G>C	XP_011535463.1:p.Trp677Cys
XM_024449713.1:c.1215G>C	XP_024305481.1:p.Trp405Cys
NM_024824.5:c.2187G>C MANE Select	NP_079100.2:p.Trp729Cys
NM_001160103.2:c.2184G>C	NP_001153575.1:p.Trp728Cys
NM_001160104.2:c.2169G>C	NP_001153576.1:p.Trp723Cys
NM_001326295.2:c.1794G>C	NP_001313224.1:p.Trp598Cys
NM_001326296.2:c.2109G>C	NP_001313225.1:p.Trp703Cys
NM_001326297.2:c.2085G>C	NP_001313226.1:p.Trp695Cys
NM_001326298.2:c.1719G>C	NP_001313227.1:p.Trp573Cys
NM_001326299.2:c.2094G>C	NP_001313228.1:p.Trp698Cys
NM_001326300.2:c.1722G>C	NP_001313229.1:p.Trp574Cys
NM_001326301.2:c.2010G>C	NP_001313230.1:p.Trp670Cys
NM_001326302.2:c.1719G>C	NP_001313231.1:p.Trp573Cys
NM_001326303.2:c.1614G>C	NP_001313232.1:p.Trp538Cys
NM_001326304.2:c.1326G>C	NP_001313233.1:p.Trp442Cys
NM_001326305.2:c.1647G>C	NP_001313234.1:p.Trp549Cys
NM_001326306.2:c.1560G>C	NP_001313235.1:p.Trp520Cys
NM_001326307.2:c.2112G>C	NP_001313236.1:p.Trp704Cys
NM_001326308.2:c.1329G>C	NP_001313237.1:p.Trp443Cys
NM_001326309.2:c.1254G>C	NP_001313238.1:p.Trp418Cys
NM_001326310.2:c.2172G>C	NP_001313239.1:p.Trp724Cys
NM_001326311.2:c.1251G>C	NP_001313240.1:p.Trp417Cys
NM_001326312.2:c.2097G>C	NP_001313241.1:p.Trp699Cys
NM_001326313.2:c.1563G>C	NP_001313242.1:p.Trp521Cys
NM_001326314.2:c.1644G>C	NP_001313243.1:p.Trp548Cys
NM_001326315.2:c.2082G>C	NP_001313244.1:p.Trp694Cys
NM_207660.4:c.1716G>C	NP_997543.1:p.Trp572Cys
NM_207662.4:c.897G>C	NP_997545.2:p.Trp299Cys
NR_136936.2:n.2124G>C
NM_001326316.2:c.2082G>C	NP_001313245.1:p.Trp694Cys
NM_207661.3:c.1692G>C	NP_997544.1:p.Trp564Cys