Canonical Allele Identifier: CA390566071
Gene: ZC3H14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88610885C>T , CM000676.2:g.88610885C>T GRCh38
NC_000014.8:g.89077229C>T , CM000676.1:g.89077229C>T GRCh37
NC_000014.7:g.88146982C>T NCBI36
NG_050601.1:g.52977C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251038.10:c.2149C>T MANE Select ENSP00000251038.5:p.Pro717Ser
ENST00000649731.1:c.*1357C>T ENSP00000497757.1:n.*1357C>T
ENST00000251038.9:c.2149C>T ENSP00000251038.5:p.Pro717Ser
ENST00000302216.12:c.1678C>T ENSP00000307025.8:p.Pro560Ser
ENST00000318308.10:c.859C>T ENSP00000327176.6:p.Pro287Ser
ENST00000336693.8:c.1654C>T ENSP00000338002.4:p.Pro552Ser
ENST00000393514.9:c.2074C>T ENSP00000377150.5:p.Pro692Ser
ENST00000406216.7:c.787C>T ENSP00000384682.3:p.Pro263Ser
ENST00000554020.5:n.992C>T
ENST00000555755.5:c.2131C>T ENSP00000452475.1:p.Pro711Ser
ENST00000555792.1:c.394C>T ENSP00000450823.1:p.Pro132Ser
ENST00000555851.6:n.308C>T
ENST00000555900.5:c.1255C>T ENSP00000451530.1:p.Pro419Ser
ENST00000556000.5:c.1893C>T
ENST00000556945.5:c.1756C>T ENSP00000450474.1:p.Pro586Ser
ENST00000557491.1:n.1434C>T
ENST00000557607.5:c.1201C>T ENSP00000452370.1:p.Pro401Ser
NM_001160103.1:c.2146C>T NP_001153575.1:p.Pro716Ser
NM_001160104.1:c.2131C>T NP_001153576.1:p.Pro711Ser
NM_024824.4:c.2149C>T NP_079100.2:p.Pro717Ser
NM_207660.3:c.1678C>T NP_997543.1:p.Pro560Ser
NM_207661.2:c.1654C>T NP_997544.1:p.Pro552Ser
NM_207662.3:c.859C>T NP_997545.2:p.Pro287Ser
XM_005268067.3:c.2134C>T XP_005268124.1:p.Pro712Ser
XM_005268068.3:c.2074C>T XP_005268125.1:p.Pro692Ser
XM_005268069.3:c.1756C>T XP_005268126.1:p.Pro586Ser
XM_005268070.3:c.1753C>T XP_005268127.1:p.Pro585Ser
XM_005268071.3:c.1681C>T XP_005268128.1:p.Pro561Ser
XM_005268073.3:c.1255C>T XP_005268130.1:p.Pro419Ser
XM_006720257.2:c.1180C>T XP_006720320.1:p.Pro394Ser
XM_011537160.1:c.2047C>T XP_011535462.1:p.Pro683Ser
XM_011537161.1:c.1993C>T XP_011535463.1:p.Pro665Ser
NM_001326295.1:c.1756C>T NP_001313224.1:p.Pro586Ser
NM_001326296.1:c.2071C>T NP_001313225.1:p.Pro691Ser
NM_001326297.1:c.2047C>T NP_001313226.1:p.Pro683Ser
NM_001326298.1:c.1681C>T NP_001313227.1:p.Pro561Ser
NM_001326299.1:c.2056C>T NP_001313228.1:p.Pro686Ser
NM_001326300.1:c.1684C>T NP_001313229.1:p.Pro562Ser
NM_001326301.1:c.1972C>T NP_001313230.1:p.Pro658Ser
NM_001326302.1:c.1681C>T NP_001313231.1:p.Pro561Ser
NM_001326303.1:c.1576C>T NP_001313232.1:p.Pro526Ser
NM_001326304.1:c.1288C>T NP_001313233.1:p.Pro430Ser
NM_001326305.1:c.1609C>T NP_001313234.1:p.Pro537Ser
NM_001326306.1:c.1522C>T NP_001313235.1:p.Pro508Ser
NM_001326307.1:c.2074C>T NP_001313236.1:p.Pro692Ser
NM_001326308.1:c.1291C>T NP_001313237.1:p.Pro431Ser
NM_001326309.1:c.1216C>T NP_001313238.1:p.Pro406Ser
NM_001326310.1:c.2134C>T NP_001313239.1:p.Pro712Ser
NM_001326311.1:c.1213C>T NP_001313240.1:p.Pro405Ser
NM_001326312.1:c.2059C>T NP_001313241.1:p.Pro687Ser
NM_001326313.1:c.1525C>T NP_001313242.1:p.Pro509Ser
NM_001326314.1:c.1606C>T NP_001313243.1:p.Pro536Ser
NM_001326315.1:c.2044C>T NP_001313244.1:p.Pro682Ser
NM_001326316.1:c.2044C>T NP_001313245.1:p.Pro682Ser
NR_136936.1:n.2214C>T
XM_005268070.5:c.1753C>T XP_005268127.1:p.Pro585Ser
XM_005268073.4:c.1255C>T XP_005268130.1:p.Pro419Ser
XM_006720257.3:c.1180C>T XP_006720320.1:p.Pro394Ser
XM_011537161.3:c.1993C>T XP_011535463.1:p.Pro665Ser
XM_024449713.1:c.1177C>T XP_024305481.1:p.Pro393Ser
NM_024824.5:c.2149C>T MANE Select NP_079100.2:p.Pro717Ser
NM_001160103.2:c.2146C>T NP_001153575.1:p.Pro716Ser
NM_001160104.2:c.2131C>T NP_001153576.1:p.Pro711Ser
NM_001326295.2:c.1756C>T NP_001313224.1:p.Pro586Ser
NM_001326296.2:c.2071C>T NP_001313225.1:p.Pro691Ser
NM_001326297.2:c.2047C>T NP_001313226.1:p.Pro683Ser
NM_001326298.2:c.1681C>T NP_001313227.1:p.Pro561Ser
NM_001326299.2:c.2056C>T NP_001313228.1:p.Pro686Ser
NM_001326300.2:c.1684C>T NP_001313229.1:p.Pro562Ser
NM_001326301.2:c.1972C>T NP_001313230.1:p.Pro658Ser
NM_001326302.2:c.1681C>T NP_001313231.1:p.Pro561Ser
NM_001326303.2:c.1576C>T NP_001313232.1:p.Pro526Ser
NM_001326304.2:c.1288C>T NP_001313233.1:p.Pro430Ser
NM_001326305.2:c.1609C>T NP_001313234.1:p.Pro537Ser
NM_001326306.2:c.1522C>T NP_001313235.1:p.Pro508Ser
NM_001326307.2:c.2074C>T NP_001313236.1:p.Pro692Ser
NM_001326308.2:c.1291C>T NP_001313237.1:p.Pro431Ser
NM_001326309.2:c.1216C>T NP_001313238.1:p.Pro406Ser
NM_001326310.2:c.2134C>T NP_001313239.1:p.Pro712Ser
NM_001326311.2:c.1213C>T NP_001313240.1:p.Pro405Ser
NM_001326312.2:c.2059C>T NP_001313241.1:p.Pro687Ser
NM_001326313.2:c.1525C>T NP_001313242.1:p.Pro509Ser
NM_001326314.2:c.1606C>T NP_001313243.1:p.Pro536Ser
NM_001326315.2:c.2044C>T NP_001313244.1:p.Pro682Ser
NM_207660.4:c.1678C>T NP_997543.1:p.Pro560Ser
NM_207662.4:c.859C>T NP_997545.2:p.Pro287Ser
NR_136936.2:n.2086C>T
NM_001326316.2:c.2044C>T NP_001313245.1:p.Pro682Ser
NM_207661.3:c.1654C>T NP_997544.1:p.Pro552Ser