Canonical Allele Identifier: CA390566032
Gene: ZC3H14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88610881C>G , CM000676.2:g.88610881C>G GRCh38
NC_000014.8:g.89077225C>G , CM000676.1:g.89077225C>G GRCh37
NC_000014.7:g.88146978C>G NCBI36
NG_050601.1:g.52973C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251038.10:c.2145C>G MANE Select ENSP00000251038.5:p.Tyr715Ter
ENST00000649731.1:c.*1353C>G ENSP00000497757.1:n.*1353C>G
ENST00000251038.9:c.2145C>G ENSP00000251038.5:p.Tyr715Ter
ENST00000302216.12:c.1674C>G ENSP00000307025.8:p.Tyr558Ter
ENST00000318308.10:c.855C>G ENSP00000327176.6:p.Tyr285Ter
ENST00000336693.8:c.1650C>G ENSP00000338002.4:p.Tyr550Ter
ENST00000393514.9:c.2070C>G ENSP00000377150.5:p.Tyr690Ter
ENST00000406216.7:c.783C>G ENSP00000384682.3:p.Tyr261Ter
ENST00000554020.5:n.988C>G
ENST00000555755.5:c.2127C>G ENSP00000452475.1:p.Tyr709Ter
ENST00000555792.1:c.390C>G ENSP00000450823.1:p.Tyr130Ter
ENST00000555851.6:n.304C>G
ENST00000555900.5:c.1251C>G ENSP00000451530.1:p.Tyr417Ter
ENST00000556000.5:c.1889C>G
ENST00000556945.5:c.1752C>G ENSP00000450474.1:p.Tyr584Ter
ENST00000557491.1:n.1430C>G
ENST00000557607.5:c.1197C>G ENSP00000452370.1:p.Tyr399Ter
NM_001160103.1:c.2142C>G NP_001153575.1:p.Tyr714Ter
NM_001160104.1:c.2127C>G NP_001153576.1:p.Tyr709Ter
NM_024824.4:c.2145C>G NP_079100.2:p.Tyr715Ter
NM_207660.3:c.1674C>G NP_997543.1:p.Tyr558Ter
NM_207661.2:c.1650C>G NP_997544.1:p.Tyr550Ter
NM_207662.3:c.855C>G NP_997545.2:p.Tyr285Ter
XM_005268067.3:c.2130C>G XP_005268124.1:p.Tyr710Ter
XM_005268068.3:c.2070C>G XP_005268125.1:p.Tyr690Ter
XM_005268069.3:c.1752C>G XP_005268126.1:p.Tyr584Ter
XM_005268070.3:c.1749C>G XP_005268127.1:p.Tyr583Ter
XM_005268071.3:c.1677C>G XP_005268128.1:p.Tyr559Ter
XM_005268073.3:c.1251C>G XP_005268130.1:p.Tyr417Ter
XM_006720257.2:c.1176C>G XP_006720320.1:p.Tyr392Ter
XM_011537160.1:c.2043C>G XP_011535462.1:p.Tyr681Ter
XM_011537161.1:c.1989C>G XP_011535463.1:p.Tyr663Ter
NM_001326295.1:c.1752C>G NP_001313224.1:p.Tyr584Ter
NM_001326296.1:c.2067C>G NP_001313225.1:p.Tyr689Ter
NM_001326297.1:c.2043C>G NP_001313226.1:p.Tyr681Ter
NM_001326298.1:c.1677C>G NP_001313227.1:p.Tyr559Ter
NM_001326299.1:c.2052C>G NP_001313228.1:p.Tyr684Ter
NM_001326300.1:c.1680C>G NP_001313229.1:p.Tyr560Ter
NM_001326301.1:c.1968C>G NP_001313230.1:p.Tyr656Ter
NM_001326302.1:c.1677C>G NP_001313231.1:p.Tyr559Ter
NM_001326303.1:c.1572C>G NP_001313232.1:p.Tyr524Ter
NM_001326304.1:c.1284C>G NP_001313233.1:p.Tyr428Ter
NM_001326305.1:c.1605C>G NP_001313234.1:p.Tyr535Ter
NM_001326306.1:c.1518C>G NP_001313235.1:p.Tyr506Ter
NM_001326307.1:c.2070C>G NP_001313236.1:p.Tyr690Ter
NM_001326308.1:c.1287C>G NP_001313237.1:p.Tyr429Ter
NM_001326309.1:c.1212C>G NP_001313238.1:p.Tyr404Ter
NM_001326310.1:c.2130C>G NP_001313239.1:p.Tyr710Ter
NM_001326311.1:c.1209C>G NP_001313240.1:p.Tyr403Ter
NM_001326312.1:c.2055C>G NP_001313241.1:p.Tyr685Ter
NM_001326313.1:c.1521C>G NP_001313242.1:p.Tyr507Ter
NM_001326314.1:c.1602C>G NP_001313243.1:p.Tyr534Ter
NM_001326315.1:c.2040C>G NP_001313244.1:p.Tyr680Ter
NM_001326316.1:c.2040C>G NP_001313245.1:p.Tyr680Ter
NR_136936.1:n.2210C>G
XM_005268070.5:c.1749C>G XP_005268127.1:p.Tyr583Ter
XM_005268073.4:c.1251C>G XP_005268130.1:p.Tyr417Ter
XM_006720257.3:c.1176C>G XP_006720320.1:p.Tyr392Ter
XM_011537161.3:c.1989C>G XP_011535463.1:p.Tyr663Ter
XM_024449713.1:c.1173C>G XP_024305481.1:p.Tyr391Ter
NM_024824.5:c.2145C>G MANE Select NP_079100.2:p.Tyr715Ter
NM_001160103.2:c.2142C>G NP_001153575.1:p.Tyr714Ter
NM_001160104.2:c.2127C>G NP_001153576.1:p.Tyr709Ter
NM_001326295.2:c.1752C>G NP_001313224.1:p.Tyr584Ter
NM_001326296.2:c.2067C>G NP_001313225.1:p.Tyr689Ter
NM_001326297.2:c.2043C>G NP_001313226.1:p.Tyr681Ter
NM_001326298.2:c.1677C>G NP_001313227.1:p.Tyr559Ter
NM_001326299.2:c.2052C>G NP_001313228.1:p.Tyr684Ter
NM_001326300.2:c.1680C>G NP_001313229.1:p.Tyr560Ter
NM_001326301.2:c.1968C>G NP_001313230.1:p.Tyr656Ter
NM_001326302.2:c.1677C>G NP_001313231.1:p.Tyr559Ter
NM_001326303.2:c.1572C>G NP_001313232.1:p.Tyr524Ter
NM_001326304.2:c.1284C>G NP_001313233.1:p.Tyr428Ter
NM_001326305.2:c.1605C>G NP_001313234.1:p.Tyr535Ter
NM_001326306.2:c.1518C>G NP_001313235.1:p.Tyr506Ter
NM_001326307.2:c.2070C>G NP_001313236.1:p.Tyr690Ter
NM_001326308.2:c.1287C>G NP_001313237.1:p.Tyr429Ter
NM_001326309.2:c.1212C>G NP_001313238.1:p.Tyr404Ter
NM_001326310.2:c.2130C>G NP_001313239.1:p.Tyr710Ter
NM_001326311.2:c.1209C>G NP_001313240.1:p.Tyr403Ter
NM_001326312.2:c.2055C>G NP_001313241.1:p.Tyr685Ter
NM_001326313.2:c.1521C>G NP_001313242.1:p.Tyr507Ter
NM_001326314.2:c.1602C>G NP_001313243.1:p.Tyr534Ter
NM_001326315.2:c.2040C>G NP_001313244.1:p.Tyr680Ter
NM_207660.4:c.1674C>G NP_997543.1:p.Tyr558Ter
NM_207662.4:c.855C>G NP_997545.2:p.Tyr285Ter
NR_136936.2:n.2082C>G
NM_001326316.2:c.2040C>G NP_001313245.1:p.Tyr680Ter
NM_207661.3:c.1650C>G NP_997544.1:p.Tyr550Ter