Canonical Allele Identifier: CA487280422
Gene: ZC3H14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.89077210G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88610866G>T , CM000676.2:g.88610866G>T GRCh38
NC_000014.8:g.89077210G>T , CM000676.1:g.89077210G>T GRCh37
NC_000014.7:g.88146963G>T NCBI36
NG_050601.1:g.52958G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251038.10:c.2130G>T MANE Select ENSP00000251038.5:p.Pro710=
ENST00000649731.1:c.*1338G>T ENSP00000497757.1:n.*1338G>T
ENST00000251038.9:c.2130G>T ENSP00000251038.5:p.Pro710=
ENST00000302216.12:c.1659G>T ENSP00000307025.8:p.Pro553=
ENST00000318308.10:c.840G>T ENSP00000327176.6:p.Pro280=
ENST00000336693.8:c.1635G>T ENSP00000338002.4:p.Pro545=
ENST00000393514.9:c.2055G>T ENSP00000377150.5:p.Pro685=
ENST00000406216.7:c.768G>T ENSP00000384682.3:p.Pro256=
ENST00000554020.5:n.973G>T
ENST00000555755.5:c.2112G>T ENSP00000452475.1:p.Pro704=
ENST00000555792.1:c.375G>T ENSP00000450823.1:p.Pro125=
ENST00000555851.6:n.289G>T
ENST00000555900.5:c.1236G>T ENSP00000451530.1:p.Pro412=
ENST00000556000.5:c.1874G>T
ENST00000556945.5:c.1737G>T ENSP00000450474.1:p.Pro579=
ENST00000557491.1:n.1415G>T
ENST00000557607.5:c.1182G>T ENSP00000452370.1:p.Pro394=
NM_001160103.1:c.2127G>T NP_001153575.1:p.Pro709=
NM_001160104.1:c.2112G>T NP_001153576.1:p.Pro704=
NM_024824.4:c.2130G>T NP_079100.2:p.Pro710=
NM_207660.3:c.1659G>T NP_997543.1:p.Pro553=
NM_207661.2:c.1635G>T NP_997544.1:p.Pro545=
NM_207662.3:c.840G>T NP_997545.2:p.Pro280=
XM_005268067.3:c.2115G>T XP_005268124.1:p.Pro705=
XM_005268068.3:c.2055G>T XP_005268125.1:p.Pro685=
XM_005268069.3:c.1737G>T XP_005268126.1:p.Pro579=
XM_005268070.3:c.1734G>T XP_005268127.1:p.Pro578=
XM_005268071.3:c.1662G>T XP_005268128.1:p.Pro554=
XM_005268073.3:c.1236G>T XP_005268130.1:p.Pro412=
XM_006720257.2:c.1161G>T XP_006720320.1:p.Pro387=
XM_011537160.1:c.2028G>T XP_011535462.1:p.Pro676=
XM_011537161.1:c.1974G>T XP_011535463.1:p.Pro658=
NM_001326295.1:c.1737G>T NP_001313224.1:p.Pro579=
NM_001326296.1:c.2052G>T NP_001313225.1:p.Pro684=
NM_001326297.1:c.2028G>T NP_001313226.1:p.Pro676=
NM_001326298.1:c.1662G>T NP_001313227.1:p.Pro554=
NM_001326299.1:c.2037G>T NP_001313228.1:p.Pro679=
NM_001326300.1:c.1665G>T NP_001313229.1:p.Pro555=
NM_001326301.1:c.1953G>T NP_001313230.1:p.Pro651=
NM_001326302.1:c.1662G>T NP_001313231.1:p.Pro554=
NM_001326303.1:c.1557G>T NP_001313232.1:p.Pro519=
NM_001326304.1:c.1269G>T NP_001313233.1:p.Pro423=
NM_001326305.1:c.1590G>T NP_001313234.1:p.Pro530=
NM_001326306.1:c.1503G>T NP_001313235.1:p.Pro501=
NM_001326307.1:c.2055G>T NP_001313236.1:p.Pro685=
NM_001326308.1:c.1272G>T NP_001313237.1:p.Pro424=
NM_001326309.1:c.1197G>T NP_001313238.1:p.Pro399=
NM_001326310.1:c.2115G>T NP_001313239.1:p.Pro705=
NM_001326311.1:c.1194G>T NP_001313240.1:p.Pro398=
NM_001326312.1:c.2040G>T NP_001313241.1:p.Pro680=
NM_001326313.1:c.1506G>T NP_001313242.1:p.Pro502=
NM_001326314.1:c.1587G>T NP_001313243.1:p.Pro529=
NM_001326315.1:c.2025G>T NP_001313244.1:p.Pro675=
NM_001326316.1:c.2025G>T NP_001313245.1:p.Pro675=
NR_136936.1:n.2195G>T
XM_005268070.5:c.1734G>T XP_005268127.1:p.Pro578=
XM_005268073.4:c.1236G>T XP_005268130.1:p.Pro412=
XM_006720257.3:c.1161G>T XP_006720320.1:p.Pro387=
XM_011537161.3:c.1974G>T XP_011535463.1:p.Pro658=
XM_024449713.1:c.1158G>T XP_024305481.1:p.Pro386=
NM_024824.5:c.2130G>T MANE Select NP_079100.2:p.Pro710=
NM_001160103.2:c.2127G>T NP_001153575.1:p.Pro709=
NM_001160104.2:c.2112G>T NP_001153576.1:p.Pro704=
NM_001326295.2:c.1737G>T NP_001313224.1:p.Pro579=
NM_001326296.2:c.2052G>T NP_001313225.1:p.Pro684=
NM_001326297.2:c.2028G>T NP_001313226.1:p.Pro676=
NM_001326298.2:c.1662G>T NP_001313227.1:p.Pro554=
NM_001326299.2:c.2037G>T NP_001313228.1:p.Pro679=
NM_001326300.2:c.1665G>T NP_001313229.1:p.Pro555=
NM_001326301.2:c.1953G>T NP_001313230.1:p.Pro651=
NM_001326302.2:c.1662G>T NP_001313231.1:p.Pro554=
NM_001326303.2:c.1557G>T NP_001313232.1:p.Pro519=
NM_001326304.2:c.1269G>T NP_001313233.1:p.Pro423=
NM_001326305.2:c.1590G>T NP_001313234.1:p.Pro530=
NM_001326306.2:c.1503G>T NP_001313235.1:p.Pro501=
NM_001326307.2:c.2055G>T NP_001313236.1:p.Pro685=
NM_001326308.2:c.1272G>T NP_001313237.1:p.Pro424=
NM_001326309.2:c.1197G>T NP_001313238.1:p.Pro399=
NM_001326310.2:c.2115G>T NP_001313239.1:p.Pro705=
NM_001326311.2:c.1194G>T NP_001313240.1:p.Pro398=
NM_001326312.2:c.2040G>T NP_001313241.1:p.Pro680=
NM_001326313.2:c.1506G>T NP_001313242.1:p.Pro502=
NM_001326314.2:c.1587G>T NP_001313243.1:p.Pro529=
NM_001326315.2:c.2025G>T NP_001313244.1:p.Pro675=
NM_207660.4:c.1659G>T NP_997543.1:p.Pro553=
NM_207662.4:c.840G>T NP_997545.2:p.Pro280=
NR_136936.2:n.2067G>T
NM_001326316.2:c.2025G>T NP_001313245.1:p.Pro675=
NM_207661.3:c.1635G>T NP_997544.1:p.Pro545=