Canonical Allele Identifier: CA390565945

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077217A>T (hg19) ; chr14:g.88610873A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610873A>T , CM000676.2:g.88610873A>T	GRCh38
NC_000014.8:g.89077217A>T , CM000676.1:g.89077217A>T	GRCh37
NC_000014.7:g.88146970A>T	NCBI36
NG_050601.1:g.52965A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2137A>T MANE Select	ENSP00000251038.5:p.Thr713Ser
ENST00000649731.1:c.*1345A>T	ENSP00000497757.1:n.*1345A>T
ENST00000251038.9:c.2137A>T	ENSP00000251038.5:p.Thr713Ser
ENST00000302216.12:c.1666A>T	ENSP00000307025.8:p.Thr556Ser
ENST00000318308.10:c.847A>T	ENSP00000327176.6:p.Thr283Ser
ENST00000336693.8:c.1642A>T	ENSP00000338002.4:p.Thr548Ser
ENST00000393514.9:c.2062A>T	ENSP00000377150.5:p.Thr688Ser
ENST00000406216.7:c.775A>T	ENSP00000384682.3:p.Thr259Ser
ENST00000554020.5:n.980A>T
ENST00000555755.5:c.2119A>T	ENSP00000452475.1:p.Thr707Ser
ENST00000555792.1:c.382A>T	ENSP00000450823.1:p.Thr128Ser
ENST00000555851.6:n.296A>T
ENST00000555900.5:c.1243A>T	ENSP00000451530.1:p.Thr415Ser
ENST00000556000.5:c.1881A>T
ENST00000556945.5:c.1744A>T	ENSP00000450474.1:p.Thr582Ser
ENST00000557491.1:n.1422A>T
ENST00000557607.5:c.1189A>T	ENSP00000452370.1:p.Thr397Ser
NM_001160103.1:c.2134A>T	NP_001153575.1:p.Thr712Ser
NM_001160104.1:c.2119A>T	NP_001153576.1:p.Thr707Ser
NM_024824.4:c.2137A>T	NP_079100.2:p.Thr713Ser
NM_207660.3:c.1666A>T	NP_997543.1:p.Thr556Ser
NM_207661.2:c.1642A>T	NP_997544.1:p.Thr548Ser
NM_207662.3:c.847A>T	NP_997545.2:p.Thr283Ser
XM_005268067.3:c.2122A>T	XP_005268124.1:p.Thr708Ser
XM_005268068.3:c.2062A>T	XP_005268125.1:p.Thr688Ser
XM_005268069.3:c.1744A>T	XP_005268126.1:p.Thr582Ser
XM_005268070.3:c.1741A>T	XP_005268127.1:p.Thr581Ser
XM_005268071.3:c.1669A>T	XP_005268128.1:p.Thr557Ser
XM_005268073.3:c.1243A>T	XP_005268130.1:p.Thr415Ser
XM_006720257.2:c.1168A>T	XP_006720320.1:p.Thr390Ser
XM_011537160.1:c.2035A>T	XP_011535462.1:p.Thr679Ser
XM_011537161.1:c.1981A>T	XP_011535463.1:p.Thr661Ser
NM_001326295.1:c.1744A>T	NP_001313224.1:p.Thr582Ser
NM_001326296.1:c.2059A>T	NP_001313225.1:p.Thr687Ser
NM_001326297.1:c.2035A>T	NP_001313226.1:p.Thr679Ser
NM_001326298.1:c.1669A>T	NP_001313227.1:p.Thr557Ser
NM_001326299.1:c.2044A>T	NP_001313228.1:p.Thr682Ser
NM_001326300.1:c.1672A>T	NP_001313229.1:p.Thr558Ser
NM_001326301.1:c.1960A>T	NP_001313230.1:p.Thr654Ser
NM_001326302.1:c.1669A>T	NP_001313231.1:p.Thr557Ser
NM_001326303.1:c.1564A>T	NP_001313232.1:p.Thr522Ser
NM_001326304.1:c.1276A>T	NP_001313233.1:p.Thr426Ser
NM_001326305.1:c.1597A>T	NP_001313234.1:p.Thr533Ser
NM_001326306.1:c.1510A>T	NP_001313235.1:p.Thr504Ser
NM_001326307.1:c.2062A>T	NP_001313236.1:p.Thr688Ser
NM_001326308.1:c.1279A>T	NP_001313237.1:p.Thr427Ser
NM_001326309.1:c.1204A>T	NP_001313238.1:p.Thr402Ser
NM_001326310.1:c.2122A>T	NP_001313239.1:p.Thr708Ser
NM_001326311.1:c.1201A>T	NP_001313240.1:p.Thr401Ser
NM_001326312.1:c.2047A>T	NP_001313241.1:p.Thr683Ser
NM_001326313.1:c.1513A>T	NP_001313242.1:p.Thr505Ser
NM_001326314.1:c.1594A>T	NP_001313243.1:p.Thr532Ser
NM_001326315.1:c.2032A>T	NP_001313244.1:p.Thr678Ser
NM_001326316.1:c.2032A>T	NP_001313245.1:p.Thr678Ser
NR_136936.1:n.2202A>T
XM_005268070.5:c.1741A>T	XP_005268127.1:p.Thr581Ser
XM_005268073.4:c.1243A>T	XP_005268130.1:p.Thr415Ser
XM_006720257.3:c.1168A>T	XP_006720320.1:p.Thr390Ser
XM_011537161.3:c.1981A>T	XP_011535463.1:p.Thr661Ser
XM_024449713.1:c.1165A>T	XP_024305481.1:p.Thr389Ser
NM_024824.5:c.2137A>T MANE Select	NP_079100.2:p.Thr713Ser
NM_001160103.2:c.2134A>T	NP_001153575.1:p.Thr712Ser
NM_001160104.2:c.2119A>T	NP_001153576.1:p.Thr707Ser
NM_001326295.2:c.1744A>T	NP_001313224.1:p.Thr582Ser
NM_001326296.2:c.2059A>T	NP_001313225.1:p.Thr687Ser
NM_001326297.2:c.2035A>T	NP_001313226.1:p.Thr679Ser
NM_001326298.2:c.1669A>T	NP_001313227.1:p.Thr557Ser
NM_001326299.2:c.2044A>T	NP_001313228.1:p.Thr682Ser
NM_001326300.2:c.1672A>T	NP_001313229.1:p.Thr558Ser
NM_001326301.2:c.1960A>T	NP_001313230.1:p.Thr654Ser
NM_001326302.2:c.1669A>T	NP_001313231.1:p.Thr557Ser
NM_001326303.2:c.1564A>T	NP_001313232.1:p.Thr522Ser
NM_001326304.2:c.1276A>T	NP_001313233.1:p.Thr426Ser
NM_001326305.2:c.1597A>T	NP_001313234.1:p.Thr533Ser
NM_001326306.2:c.1510A>T	NP_001313235.1:p.Thr504Ser
NM_001326307.2:c.2062A>T	NP_001313236.1:p.Thr688Ser
NM_001326308.2:c.1279A>T	NP_001313237.1:p.Thr427Ser
NM_001326309.2:c.1204A>T	NP_001313238.1:p.Thr402Ser
NM_001326310.2:c.2122A>T	NP_001313239.1:p.Thr708Ser
NM_001326311.2:c.1201A>T	NP_001313240.1:p.Thr401Ser
NM_001326312.2:c.2047A>T	NP_001313241.1:p.Thr683Ser
NM_001326313.2:c.1513A>T	NP_001313242.1:p.Thr505Ser
NM_001326314.2:c.1594A>T	NP_001313243.1:p.Thr532Ser
NM_001326315.2:c.2032A>T	NP_001313244.1:p.Thr678Ser
NM_207660.4:c.1666A>T	NP_997543.1:p.Thr556Ser
NM_207662.4:c.847A>T	NP_997545.2:p.Thr283Ser
NR_136936.2:n.2074A>T
NM_001326316.2:c.2032A>T	NP_001313245.1:p.Thr678Ser
NM_207661.3:c.1642A>T	NP_997544.1:p.Thr548Ser