Canonical Allele Identifier: CA390566480
Gene: ZC3H14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88610936A>G , CM000676.2:g.88610936A>G GRCh38
NC_000014.8:g.89077280A>G , CM000676.1:g.89077280A>G GRCh37
NC_000014.7:g.88147033A>G NCBI36
NG_050601.1:g.53028A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251038.10:c.2200A>G MANE Select ENSP00000251038.5:p.Thr734Ala
ENST00000649731.1:c.*1408A>G ENSP00000497757.1:n.*1408A>G
ENST00000251038.9:c.2200A>G ENSP00000251038.5:p.Thr734Ala
ENST00000302216.12:c.1729A>G ENSP00000307025.8:p.Thr577Ala
ENST00000318308.10:c.910A>G ENSP00000327176.6:p.Thr304Ala
ENST00000336693.8:c.1705A>G ENSP00000338002.4:p.Thr569Ala
ENST00000393514.9:c.2125A>G ENSP00000377150.5:p.Thr709Ala
ENST00000406216.7:c.838A>G ENSP00000384682.3:p.Thr280Ala
ENST00000554020.5:n.1043A>G
ENST00000555755.5:c.2182A>G ENSP00000452475.1:p.Thr728Ala
ENST00000555792.1:c.445A>G ENSP00000450823.1:p.Thr149Ala
ENST00000555851.6:n.359A>G
ENST00000555900.5:c.1306A>G ENSP00000451530.1:p.Thr436Ala
ENST00000556000.5:c.1944A>G
ENST00000556945.5:c.1807A>G ENSP00000450474.1:p.Thr603Ala
ENST00000557491.1:n.1485A>G
ENST00000557607.5:c.1252A>G ENSP00000452370.1:p.Thr418Ala
NM_001160103.1:c.2197A>G NP_001153575.1:p.Thr733Ala
NM_001160104.1:c.2182A>G NP_001153576.1:p.Thr728Ala
NM_024824.4:c.2200A>G NP_079100.2:p.Thr734Ala
NM_207660.3:c.1729A>G NP_997543.1:p.Thr577Ala
NM_207661.2:c.1705A>G NP_997544.1:p.Thr569Ala
NM_207662.3:c.910A>G NP_997545.2:p.Thr304Ala
XM_005268067.3:c.2185A>G XP_005268124.1:p.Thr729Ala
XM_005268068.3:c.2125A>G XP_005268125.1:p.Thr709Ala
XM_005268069.3:c.1807A>G XP_005268126.1:p.Thr603Ala
XM_005268070.3:c.1804A>G XP_005268127.1:p.Thr602Ala
XM_005268071.3:c.1732A>G XP_005268128.1:p.Thr578Ala
XM_005268073.3:c.1306A>G XP_005268130.1:p.Thr436Ala
XM_006720257.2:c.1231A>G XP_006720320.1:p.Thr411Ala
XM_011537160.1:c.2098A>G XP_011535462.1:p.Thr700Ala
XM_011537161.1:c.2044A>G XP_011535463.1:p.Thr682Ala
NM_001326295.1:c.1807A>G NP_001313224.1:p.Thr603Ala
NM_001326296.1:c.2122A>G NP_001313225.1:p.Thr708Ala
NM_001326297.1:c.2098A>G NP_001313226.1:p.Thr700Ala
NM_001326298.1:c.1732A>G NP_001313227.1:p.Thr578Ala
NM_001326299.1:c.2107A>G NP_001313228.1:p.Thr703Ala
NM_001326300.1:c.1735A>G NP_001313229.1:p.Thr579Ala
NM_001326301.1:c.2023A>G NP_001313230.1:p.Thr675Ala
NM_001326302.1:c.1732A>G NP_001313231.1:p.Thr578Ala
NM_001326303.1:c.1627A>G NP_001313232.1:p.Thr543Ala
NM_001326304.1:c.1339A>G NP_001313233.1:p.Thr447Ala
NM_001326305.1:c.1660A>G NP_001313234.1:p.Thr554Ala
NM_001326306.1:c.1573A>G NP_001313235.1:p.Thr525Ala
NM_001326307.1:c.2125A>G NP_001313236.1:p.Thr709Ala
NM_001326308.1:c.1342A>G NP_001313237.1:p.Thr448Ala
NM_001326309.1:c.1267A>G NP_001313238.1:p.Thr423Ala
NM_001326310.1:c.2185A>G NP_001313239.1:p.Thr729Ala
NM_001326311.1:c.1264A>G NP_001313240.1:p.Thr422Ala
NM_001326312.1:c.2110A>G NP_001313241.1:p.Thr704Ala
NM_001326313.1:c.1576A>G NP_001313242.1:p.Thr526Ala
NM_001326314.1:c.1657A>G NP_001313243.1:p.Thr553Ala
NM_001326315.1:c.2095A>G NP_001313244.1:p.Thr699Ala
NM_001326316.1:c.2095A>G NP_001313245.1:p.Thr699Ala
NR_136936.1:n.2265A>G
XM_005268070.5:c.1804A>G XP_005268127.1:p.Thr602Ala
XM_005268073.4:c.1306A>G XP_005268130.1:p.Thr436Ala
XM_006720257.3:c.1231A>G XP_006720320.1:p.Thr411Ala
XM_011537161.3:c.2044A>G XP_011535463.1:p.Thr682Ala
XM_024449713.1:c.1228A>G XP_024305481.1:p.Thr410Ala
NM_024824.5:c.2200A>G MANE Select NP_079100.2:p.Thr734Ala
NM_001160103.2:c.2197A>G NP_001153575.1:p.Thr733Ala
NM_001160104.2:c.2182A>G NP_001153576.1:p.Thr728Ala
NM_001326295.2:c.1807A>G NP_001313224.1:p.Thr603Ala
NM_001326296.2:c.2122A>G NP_001313225.1:p.Thr708Ala
NM_001326297.2:c.2098A>G NP_001313226.1:p.Thr700Ala
NM_001326298.2:c.1732A>G NP_001313227.1:p.Thr578Ala
NM_001326299.2:c.2107A>G NP_001313228.1:p.Thr703Ala
NM_001326300.2:c.1735A>G NP_001313229.1:p.Thr579Ala
NM_001326301.2:c.2023A>G NP_001313230.1:p.Thr675Ala
NM_001326302.2:c.1732A>G NP_001313231.1:p.Thr578Ala
NM_001326303.2:c.1627A>G NP_001313232.1:p.Thr543Ala
NM_001326304.2:c.1339A>G NP_001313233.1:p.Thr447Ala
NM_001326305.2:c.1660A>G NP_001313234.1:p.Thr554Ala
NM_001326306.2:c.1573A>G NP_001313235.1:p.Thr525Ala
NM_001326307.2:c.2125A>G NP_001313236.1:p.Thr709Ala
NM_001326308.2:c.1342A>G NP_001313237.1:p.Thr448Ala
NM_001326309.2:c.1267A>G NP_001313238.1:p.Thr423Ala
NM_001326310.2:c.2185A>G NP_001313239.1:p.Thr729Ala
NM_001326311.2:c.1264A>G NP_001313240.1:p.Thr422Ala
NM_001326312.2:c.2110A>G NP_001313241.1:p.Thr704Ala
NM_001326313.2:c.1576A>G NP_001313242.1:p.Thr526Ala
NM_001326314.2:c.1657A>G NP_001313243.1:p.Thr553Ala
NM_001326315.2:c.2095A>G NP_001313244.1:p.Thr699Ala
NM_207660.4:c.1729A>G NP_997543.1:p.Thr577Ala
NM_207662.4:c.910A>G NP_997545.2:p.Thr304Ala
NR_136936.2:n.2137A>G
NM_001326316.2:c.2095A>G NP_001313245.1:p.Thr699Ala
NM_207661.3:c.1705A>G NP_997544.1:p.Thr569Ala