Canonical Allele Identifier: CA487280437

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077234C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610890C>G , CM000676.2:g.88610890C>G	GRCh38
NC_000014.8:g.89077234C>G , CM000676.1:g.89077234C>G	GRCh37
NC_000014.7:g.88146987C>G	NCBI36
NG_050601.1:g.52982C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2154C>G MANE Select	ENSP00000251038.5:p.Thr718=
ENST00000649731.1:c.*1362C>G	ENSP00000497757.1:n.*1362C>G
ENST00000251038.9:c.2154C>G	ENSP00000251038.5:p.Thr718=
ENST00000302216.12:c.1683C>G	ENSP00000307025.8:p.Thr561=
ENST00000318308.10:c.864C>G	ENSP00000327176.6:p.Thr288=
ENST00000336693.8:c.1659C>G	ENSP00000338002.4:p.Thr553=
ENST00000393514.9:c.2079C>G	ENSP00000377150.5:p.Thr693=
ENST00000406216.7:c.792C>G	ENSP00000384682.3:p.Thr264=
ENST00000554020.5:n.997C>G
ENST00000555755.5:c.2136C>G	ENSP00000452475.1:p.Thr712=
ENST00000555792.1:c.399C>G	ENSP00000450823.1:p.Thr133=
ENST00000555851.6:n.313C>G
ENST00000555900.5:c.1260C>G	ENSP00000451530.1:p.Thr420=
ENST00000556000.5:c.1898C>G
ENST00000556945.5:c.1761C>G	ENSP00000450474.1:p.Thr587=
ENST00000557491.1:n.1439C>G
ENST00000557607.5:c.1206C>G	ENSP00000452370.1:p.Thr402=
NM_001160103.1:c.2151C>G	NP_001153575.1:p.Thr717=
NM_001160104.1:c.2136C>G	NP_001153576.1:p.Thr712=
NM_024824.4:c.2154C>G	NP_079100.2:p.Thr718=
NM_207660.3:c.1683C>G	NP_997543.1:p.Thr561=
NM_207661.2:c.1659C>G	NP_997544.1:p.Thr553=
NM_207662.3:c.864C>G	NP_997545.2:p.Thr288=
XM_005268067.3:c.2139C>G	XP_005268124.1:p.Thr713=
XM_005268068.3:c.2079C>G	XP_005268125.1:p.Thr693=
XM_005268069.3:c.1761C>G	XP_005268126.1:p.Thr587=
XM_005268070.3:c.1758C>G	XP_005268127.1:p.Thr586=
XM_005268071.3:c.1686C>G	XP_005268128.1:p.Thr562=
XM_005268073.3:c.1260C>G	XP_005268130.1:p.Thr420=
XM_006720257.2:c.1185C>G	XP_006720320.1:p.Thr395=
XM_011537160.1:c.2052C>G	XP_011535462.1:p.Thr684=
XM_011537161.1:c.1998C>G	XP_011535463.1:p.Thr666=
NM_001326295.1:c.1761C>G	NP_001313224.1:p.Thr587=
NM_001326296.1:c.2076C>G	NP_001313225.1:p.Thr692=
NM_001326297.1:c.2052C>G	NP_001313226.1:p.Thr684=
NM_001326298.1:c.1686C>G	NP_001313227.1:p.Thr562=
NM_001326299.1:c.2061C>G	NP_001313228.1:p.Thr687=
NM_001326300.1:c.1689C>G	NP_001313229.1:p.Thr563=
NM_001326301.1:c.1977C>G	NP_001313230.1:p.Thr659=
NM_001326302.1:c.1686C>G	NP_001313231.1:p.Thr562=
NM_001326303.1:c.1581C>G	NP_001313232.1:p.Thr527=
NM_001326304.1:c.1293C>G	NP_001313233.1:p.Thr431=
NM_001326305.1:c.1614C>G	NP_001313234.1:p.Thr538=
NM_001326306.1:c.1527C>G	NP_001313235.1:p.Thr509=
NM_001326307.1:c.2079C>G	NP_001313236.1:p.Thr693=
NM_001326308.1:c.1296C>G	NP_001313237.1:p.Thr432=
NM_001326309.1:c.1221C>G	NP_001313238.1:p.Thr407=
NM_001326310.1:c.2139C>G	NP_001313239.1:p.Thr713=
NM_001326311.1:c.1218C>G	NP_001313240.1:p.Thr406=
NM_001326312.1:c.2064C>G	NP_001313241.1:p.Thr688=
NM_001326313.1:c.1530C>G	NP_001313242.1:p.Thr510=
NM_001326314.1:c.1611C>G	NP_001313243.1:p.Thr537=
NM_001326315.1:c.2049C>G	NP_001313244.1:p.Thr683=
NM_001326316.1:c.2049C>G	NP_001313245.1:p.Thr683=
NR_136936.1:n.2219C>G
XM_005268070.5:c.1758C>G	XP_005268127.1:p.Thr586=
XM_005268073.4:c.1260C>G	XP_005268130.1:p.Thr420=
XM_006720257.3:c.1185C>G	XP_006720320.1:p.Thr395=
XM_011537161.3:c.1998C>G	XP_011535463.1:p.Thr666=
XM_024449713.1:c.1182C>G	XP_024305481.1:p.Thr394=
NM_024824.5:c.2154C>G MANE Select	NP_079100.2:p.Thr718=
NM_001160103.2:c.2151C>G	NP_001153575.1:p.Thr717=
NM_001160104.2:c.2136C>G	NP_001153576.1:p.Thr712=
NM_001326295.2:c.1761C>G	NP_001313224.1:p.Thr587=
NM_001326296.2:c.2076C>G	NP_001313225.1:p.Thr692=
NM_001326297.2:c.2052C>G	NP_001313226.1:p.Thr684=
NM_001326298.2:c.1686C>G	NP_001313227.1:p.Thr562=
NM_001326299.2:c.2061C>G	NP_001313228.1:p.Thr687=
NM_001326300.2:c.1689C>G	NP_001313229.1:p.Thr563=
NM_001326301.2:c.1977C>G	NP_001313230.1:p.Thr659=
NM_001326302.2:c.1686C>G	NP_001313231.1:p.Thr562=
NM_001326303.2:c.1581C>G	NP_001313232.1:p.Thr527=
NM_001326304.2:c.1293C>G	NP_001313233.1:p.Thr431=
NM_001326305.2:c.1614C>G	NP_001313234.1:p.Thr538=
NM_001326306.2:c.1527C>G	NP_001313235.1:p.Thr509=
NM_001326307.2:c.2079C>G	NP_001313236.1:p.Thr693=
NM_001326308.2:c.1296C>G	NP_001313237.1:p.Thr432=
NM_001326309.2:c.1221C>G	NP_001313238.1:p.Thr407=
NM_001326310.2:c.2139C>G	NP_001313239.1:p.Thr713=
NM_001326311.2:c.1218C>G	NP_001313240.1:p.Thr406=
NM_001326312.2:c.2064C>G	NP_001313241.1:p.Thr688=
NM_001326313.2:c.1530C>G	NP_001313242.1:p.Thr510=
NM_001326314.2:c.1611C>G	NP_001313243.1:p.Thr537=
NM_001326315.2:c.2049C>G	NP_001313244.1:p.Thr683=
NM_207660.4:c.1683C>G	NP_997543.1:p.Thr561=
NM_207662.4:c.864C>G	NP_997545.2:p.Thr288=
NR_136936.2:n.2091C>G
NM_001326316.2:c.2049C>G	NP_001313245.1:p.Thr683=
NM_207661.3:c.1659C>G	NP_997544.1:p.Thr553=