Canonical Allele Identifier: CA390566209
Gene: ZC3H14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88610903C>A , CM000676.2:g.88610903C>A GRCh38
NC_000014.8:g.89077247C>A , CM000676.1:g.89077247C>A GRCh37
NC_000014.7:g.88147000C>A NCBI36
NG_050601.1:g.52995C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251038.10:c.2167C>A MANE Select ENSP00000251038.5:p.Pro723Thr
ENST00000649731.1:c.*1375C>A ENSP00000497757.1:n.*1375C>A
ENST00000251038.9:c.2167C>A ENSP00000251038.5:p.Pro723Thr
ENST00000302216.12:c.1696C>A ENSP00000307025.8:p.Pro566Thr
ENST00000318308.10:c.877C>A ENSP00000327176.6:p.Pro293Thr
ENST00000336693.8:c.1672C>A ENSP00000338002.4:p.Pro558Thr
ENST00000393514.9:c.2092C>A ENSP00000377150.5:p.Pro698Thr
ENST00000406216.7:c.805C>A ENSP00000384682.3:p.Pro269Thr
ENST00000554020.5:n.1010C>A
ENST00000555755.5:c.2149C>A ENSP00000452475.1:p.Pro717Thr
ENST00000555792.1:c.412C>A ENSP00000450823.1:p.Pro138Thr
ENST00000555851.6:n.326C>A
ENST00000555900.5:c.1273C>A ENSP00000451530.1:p.Pro425Thr
ENST00000556000.5:c.1911C>A
ENST00000556945.5:c.1774C>A ENSP00000450474.1:p.Pro592Thr
ENST00000557491.1:n.1452C>A
ENST00000557607.5:c.1219C>A ENSP00000452370.1:p.Pro407Thr
NM_001160103.1:c.2164C>A NP_001153575.1:p.Pro722Thr
NM_001160104.1:c.2149C>A NP_001153576.1:p.Pro717Thr
NM_024824.4:c.2167C>A NP_079100.2:p.Pro723Thr
NM_207660.3:c.1696C>A NP_997543.1:p.Pro566Thr
NM_207661.2:c.1672C>A NP_997544.1:p.Pro558Thr
NM_207662.3:c.877C>A NP_997545.2:p.Pro293Thr
XM_005268067.3:c.2152C>A XP_005268124.1:p.Pro718Thr
XM_005268068.3:c.2092C>A XP_005268125.1:p.Pro698Thr
XM_005268069.3:c.1774C>A XP_005268126.1:p.Pro592Thr
XM_005268070.3:c.1771C>A XP_005268127.1:p.Pro591Thr
XM_005268071.3:c.1699C>A XP_005268128.1:p.Pro567Thr
XM_005268073.3:c.1273C>A XP_005268130.1:p.Pro425Thr
XM_006720257.2:c.1198C>A XP_006720320.1:p.Pro400Thr
XM_011537160.1:c.2065C>A XP_011535462.1:p.Pro689Thr
XM_011537161.1:c.2011C>A XP_011535463.1:p.Pro671Thr
NM_001326295.1:c.1774C>A NP_001313224.1:p.Pro592Thr
NM_001326296.1:c.2089C>A NP_001313225.1:p.Pro697Thr
NM_001326297.1:c.2065C>A NP_001313226.1:p.Pro689Thr
NM_001326298.1:c.1699C>A NP_001313227.1:p.Pro567Thr
NM_001326299.1:c.2074C>A NP_001313228.1:p.Pro692Thr
NM_001326300.1:c.1702C>A NP_001313229.1:p.Pro568Thr
NM_001326301.1:c.1990C>A NP_001313230.1:p.Pro664Thr
NM_001326302.1:c.1699C>A NP_001313231.1:p.Pro567Thr
NM_001326303.1:c.1594C>A NP_001313232.1:p.Pro532Thr
NM_001326304.1:c.1306C>A NP_001313233.1:p.Pro436Thr
NM_001326305.1:c.1627C>A NP_001313234.1:p.Pro543Thr
NM_001326306.1:c.1540C>A NP_001313235.1:p.Pro514Thr
NM_001326307.1:c.2092C>A NP_001313236.1:p.Pro698Thr
NM_001326308.1:c.1309C>A NP_001313237.1:p.Pro437Thr
NM_001326309.1:c.1234C>A NP_001313238.1:p.Pro412Thr
NM_001326310.1:c.2152C>A NP_001313239.1:p.Pro718Thr
NM_001326311.1:c.1231C>A NP_001313240.1:p.Pro411Thr
NM_001326312.1:c.2077C>A NP_001313241.1:p.Pro693Thr
NM_001326313.1:c.1543C>A NP_001313242.1:p.Pro515Thr
NM_001326314.1:c.1624C>A NP_001313243.1:p.Pro542Thr
NM_001326315.1:c.2062C>A NP_001313244.1:p.Pro688Thr
NM_001326316.1:c.2062C>A NP_001313245.1:p.Pro688Thr
NR_136936.1:n.2232C>A
XM_005268070.5:c.1771C>A XP_005268127.1:p.Pro591Thr
XM_005268073.4:c.1273C>A XP_005268130.1:p.Pro425Thr
XM_006720257.3:c.1198C>A XP_006720320.1:p.Pro400Thr
XM_011537161.3:c.2011C>A XP_011535463.1:p.Pro671Thr
XM_024449713.1:c.1195C>A XP_024305481.1:p.Pro399Thr
NM_024824.5:c.2167C>A MANE Select NP_079100.2:p.Pro723Thr
NM_001160103.2:c.2164C>A NP_001153575.1:p.Pro722Thr
NM_001160104.2:c.2149C>A NP_001153576.1:p.Pro717Thr
NM_001326295.2:c.1774C>A NP_001313224.1:p.Pro592Thr
NM_001326296.2:c.2089C>A NP_001313225.1:p.Pro697Thr
NM_001326297.2:c.2065C>A NP_001313226.1:p.Pro689Thr
NM_001326298.2:c.1699C>A NP_001313227.1:p.Pro567Thr
NM_001326299.2:c.2074C>A NP_001313228.1:p.Pro692Thr
NM_001326300.2:c.1702C>A NP_001313229.1:p.Pro568Thr
NM_001326301.2:c.1990C>A NP_001313230.1:p.Pro664Thr
NM_001326302.2:c.1699C>A NP_001313231.1:p.Pro567Thr
NM_001326303.2:c.1594C>A NP_001313232.1:p.Pro532Thr
NM_001326304.2:c.1306C>A NP_001313233.1:p.Pro436Thr
NM_001326305.2:c.1627C>A NP_001313234.1:p.Pro543Thr
NM_001326306.2:c.1540C>A NP_001313235.1:p.Pro514Thr
NM_001326307.2:c.2092C>A NP_001313236.1:p.Pro698Thr
NM_001326308.2:c.1309C>A NP_001313237.1:p.Pro437Thr
NM_001326309.2:c.1234C>A NP_001313238.1:p.Pro412Thr
NM_001326310.2:c.2152C>A NP_001313239.1:p.Pro718Thr
NM_001326311.2:c.1231C>A NP_001313240.1:p.Pro411Thr
NM_001326312.2:c.2077C>A NP_001313241.1:p.Pro693Thr
NM_001326313.2:c.1543C>A NP_001313242.1:p.Pro515Thr
NM_001326314.2:c.1624C>A NP_001313243.1:p.Pro542Thr
NM_001326315.2:c.2062C>A NP_001313244.1:p.Pro688Thr
NM_207660.4:c.1696C>A NP_997543.1:p.Pro566Thr
NM_207662.4:c.877C>A NP_997545.2:p.Pro293Thr
NR_136936.2:n.2104C>A
NM_001326316.2:c.2062C>A NP_001313245.1:p.Pro688Thr
NM_207661.3:c.1672C>A NP_997544.1:p.Pro558Thr