Canonical Allele Identifier: CA390566103

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077233C>G (hg19) ; chr14:g.88610889C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610889C>G , CM000676.2:g.88610889C>G	GRCh38
NC_000014.8:g.89077233C>G , CM000676.1:g.89077233C>G	GRCh37
NC_000014.7:g.88146986C>G	NCBI36
NG_050601.1:g.52981C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2153C>G MANE Select	ENSP00000251038.5:p.Thr718Ser
ENST00000649731.1:c.*1361C>G	ENSP00000497757.1:n.*1361C>G
ENST00000251038.9:c.2153C>G	ENSP00000251038.5:p.Thr718Ser
ENST00000302216.12:c.1682C>G	ENSP00000307025.8:p.Thr561Ser
ENST00000318308.10:c.863C>G	ENSP00000327176.6:p.Thr288Ser
ENST00000336693.8:c.1658C>G	ENSP00000338002.4:p.Thr553Ser
ENST00000393514.9:c.2078C>G	ENSP00000377150.5:p.Thr693Ser
ENST00000406216.7:c.791C>G	ENSP00000384682.3:p.Thr264Ser
ENST00000554020.5:n.996C>G
ENST00000555755.5:c.2135C>G	ENSP00000452475.1:p.Thr712Ser
ENST00000555792.1:c.398C>G	ENSP00000450823.1:p.Thr133Ser
ENST00000555851.6:n.312C>G
ENST00000555900.5:c.1259C>G	ENSP00000451530.1:p.Thr420Ser
ENST00000556000.5:c.1897C>G
ENST00000556945.5:c.1760C>G	ENSP00000450474.1:p.Thr587Ser
ENST00000557491.1:n.1438C>G
ENST00000557607.5:c.1205C>G	ENSP00000452370.1:p.Thr402Ser
NM_001160103.1:c.2150C>G	NP_001153575.1:p.Thr717Ser
NM_001160104.1:c.2135C>G	NP_001153576.1:p.Thr712Ser
NM_024824.4:c.2153C>G	NP_079100.2:p.Thr718Ser
NM_207660.3:c.1682C>G	NP_997543.1:p.Thr561Ser
NM_207661.2:c.1658C>G	NP_997544.1:p.Thr553Ser
NM_207662.3:c.863C>G	NP_997545.2:p.Thr288Ser
XM_005268067.3:c.2138C>G	XP_005268124.1:p.Thr713Ser
XM_005268068.3:c.2078C>G	XP_005268125.1:p.Thr693Ser
XM_005268069.3:c.1760C>G	XP_005268126.1:p.Thr587Ser
XM_005268070.3:c.1757C>G	XP_005268127.1:p.Thr586Ser
XM_005268071.3:c.1685C>G	XP_005268128.1:p.Thr562Ser
XM_005268073.3:c.1259C>G	XP_005268130.1:p.Thr420Ser
XM_006720257.2:c.1184C>G	XP_006720320.1:p.Thr395Ser
XM_011537160.1:c.2051C>G	XP_011535462.1:p.Thr684Ser
XM_011537161.1:c.1997C>G	XP_011535463.1:p.Thr666Ser
NM_001326295.1:c.1760C>G	NP_001313224.1:p.Thr587Ser
NM_001326296.1:c.2075C>G	NP_001313225.1:p.Thr692Ser
NM_001326297.1:c.2051C>G	NP_001313226.1:p.Thr684Ser
NM_001326298.1:c.1685C>G	NP_001313227.1:p.Thr562Ser
NM_001326299.1:c.2060C>G	NP_001313228.1:p.Thr687Ser
NM_001326300.1:c.1688C>G	NP_001313229.1:p.Thr563Ser
NM_001326301.1:c.1976C>G	NP_001313230.1:p.Thr659Ser
NM_001326302.1:c.1685C>G	NP_001313231.1:p.Thr562Ser
NM_001326303.1:c.1580C>G	NP_001313232.1:p.Thr527Ser
NM_001326304.1:c.1292C>G	NP_001313233.1:p.Thr431Ser
NM_001326305.1:c.1613C>G	NP_001313234.1:p.Thr538Ser
NM_001326306.1:c.1526C>G	NP_001313235.1:p.Thr509Ser
NM_001326307.1:c.2078C>G	NP_001313236.1:p.Thr693Ser
NM_001326308.1:c.1295C>G	NP_001313237.1:p.Thr432Ser
NM_001326309.1:c.1220C>G	NP_001313238.1:p.Thr407Ser
NM_001326310.1:c.2138C>G	NP_001313239.1:p.Thr713Ser
NM_001326311.1:c.1217C>G	NP_001313240.1:p.Thr406Ser
NM_001326312.1:c.2063C>G	NP_001313241.1:p.Thr688Ser
NM_001326313.1:c.1529C>G	NP_001313242.1:p.Thr510Ser
NM_001326314.1:c.1610C>G	NP_001313243.1:p.Thr537Ser
NM_001326315.1:c.2048C>G	NP_001313244.1:p.Thr683Ser
NM_001326316.1:c.2048C>G	NP_001313245.1:p.Thr683Ser
NR_136936.1:n.2218C>G
XM_005268070.5:c.1757C>G	XP_005268127.1:p.Thr586Ser
XM_005268073.4:c.1259C>G	XP_005268130.1:p.Thr420Ser
XM_006720257.3:c.1184C>G	XP_006720320.1:p.Thr395Ser
XM_011537161.3:c.1997C>G	XP_011535463.1:p.Thr666Ser
XM_024449713.1:c.1181C>G	XP_024305481.1:p.Thr394Ser
NM_024824.5:c.2153C>G MANE Select	NP_079100.2:p.Thr718Ser
NM_001160103.2:c.2150C>G	NP_001153575.1:p.Thr717Ser
NM_001160104.2:c.2135C>G	NP_001153576.1:p.Thr712Ser
NM_001326295.2:c.1760C>G	NP_001313224.1:p.Thr587Ser
NM_001326296.2:c.2075C>G	NP_001313225.1:p.Thr692Ser
NM_001326297.2:c.2051C>G	NP_001313226.1:p.Thr684Ser
NM_001326298.2:c.1685C>G	NP_001313227.1:p.Thr562Ser
NM_001326299.2:c.2060C>G	NP_001313228.1:p.Thr687Ser
NM_001326300.2:c.1688C>G	NP_001313229.1:p.Thr563Ser
NM_001326301.2:c.1976C>G	NP_001313230.1:p.Thr659Ser
NM_001326302.2:c.1685C>G	NP_001313231.1:p.Thr562Ser
NM_001326303.2:c.1580C>G	NP_001313232.1:p.Thr527Ser
NM_001326304.2:c.1292C>G	NP_001313233.1:p.Thr431Ser
NM_001326305.2:c.1613C>G	NP_001313234.1:p.Thr538Ser
NM_001326306.2:c.1526C>G	NP_001313235.1:p.Thr509Ser
NM_001326307.2:c.2078C>G	NP_001313236.1:p.Thr693Ser
NM_001326308.2:c.1295C>G	NP_001313237.1:p.Thr432Ser
NM_001326309.2:c.1220C>G	NP_001313238.1:p.Thr407Ser
NM_001326310.2:c.2138C>G	NP_001313239.1:p.Thr713Ser
NM_001326311.2:c.1217C>G	NP_001313240.1:p.Thr406Ser
NM_001326312.2:c.2063C>G	NP_001313241.1:p.Thr688Ser
NM_001326313.2:c.1529C>G	NP_001313242.1:p.Thr510Ser
NM_001326314.2:c.1610C>G	NP_001313243.1:p.Thr537Ser
NM_001326315.2:c.2048C>G	NP_001313244.1:p.Thr683Ser
NM_207660.4:c.1682C>G	NP_997543.1:p.Thr561Ser
NM_207662.4:c.863C>G	NP_997545.2:p.Thr288Ser
NR_136936.2:n.2090C>G
NM_001326316.2:c.2048C>G	NP_001313245.1:p.Thr683Ser
NM_207661.3:c.1658C>G	NP_997544.1:p.Thr553Ser