Canonical Allele Identifier: CA390566130

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077238A>T (hg19) ; chr14:g.88610894A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610894A>T , CM000676.2:g.88610894A>T	GRCh38
NC_000014.8:g.89077238A>T , CM000676.1:g.89077238A>T	GRCh37
NC_000014.7:g.88146991A>T	NCBI36
NG_050601.1:g.52986A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2158A>T MANE Select	ENSP00000251038.5:p.Asn720Tyr
ENST00000649731.1:c.*1366A>T	ENSP00000497757.1:n.*1366A>T
ENST00000251038.9:c.2158A>T	ENSP00000251038.5:p.Asn720Tyr
ENST00000302216.12:c.1687A>T	ENSP00000307025.8:p.Asn563Tyr
ENST00000318308.10:c.868A>T	ENSP00000327176.6:p.Asn290Tyr
ENST00000336693.8:c.1663A>T	ENSP00000338002.4:p.Asn555Tyr
ENST00000393514.9:c.2083A>T	ENSP00000377150.5:p.Asn695Tyr
ENST00000406216.7:c.796A>T	ENSP00000384682.3:p.Asn266Tyr
ENST00000554020.5:n.1001A>T
ENST00000555755.5:c.2140A>T	ENSP00000452475.1:p.Asn714Tyr
ENST00000555792.1:c.403A>T	ENSP00000450823.1:p.Asn135Tyr
ENST00000555851.6:n.317A>T
ENST00000555900.5:c.1264A>T	ENSP00000451530.1:p.Asn422Tyr
ENST00000556000.5:c.1902A>T
ENST00000556945.5:c.1765A>T	ENSP00000450474.1:p.Asn589Tyr
ENST00000557491.1:n.1443A>T
ENST00000557607.5:c.1210A>T	ENSP00000452370.1:p.Asn404Tyr
NM_001160103.1:c.2155A>T	NP_001153575.1:p.Asn719Tyr
NM_001160104.1:c.2140A>T	NP_001153576.1:p.Asn714Tyr
NM_024824.4:c.2158A>T	NP_079100.2:p.Asn720Tyr
NM_207660.3:c.1687A>T	NP_997543.1:p.Asn563Tyr
NM_207661.2:c.1663A>T	NP_997544.1:p.Asn555Tyr
NM_207662.3:c.868A>T	NP_997545.2:p.Asn290Tyr
XM_005268067.3:c.2143A>T	XP_005268124.1:p.Asn715Tyr
XM_005268068.3:c.2083A>T	XP_005268125.1:p.Asn695Tyr
XM_005268069.3:c.1765A>T	XP_005268126.1:p.Asn589Tyr
XM_005268070.3:c.1762A>T	XP_005268127.1:p.Asn588Tyr
XM_005268071.3:c.1690A>T	XP_005268128.1:p.Asn564Tyr
XM_005268073.3:c.1264A>T	XP_005268130.1:p.Asn422Tyr
XM_006720257.2:c.1189A>T	XP_006720320.1:p.Asn397Tyr
XM_011537160.1:c.2056A>T	XP_011535462.1:p.Asn686Tyr
XM_011537161.1:c.2002A>T	XP_011535463.1:p.Asn668Tyr
NM_001326295.1:c.1765A>T	NP_001313224.1:p.Asn589Tyr
NM_001326296.1:c.2080A>T	NP_001313225.1:p.Asn694Tyr
NM_001326297.1:c.2056A>T	NP_001313226.1:p.Asn686Tyr
NM_001326298.1:c.1690A>T	NP_001313227.1:p.Asn564Tyr
NM_001326299.1:c.2065A>T	NP_001313228.1:p.Asn689Tyr
NM_001326300.1:c.1693A>T	NP_001313229.1:p.Asn565Tyr
NM_001326301.1:c.1981A>T	NP_001313230.1:p.Asn661Tyr
NM_001326302.1:c.1690A>T	NP_001313231.1:p.Asn564Tyr
NM_001326303.1:c.1585A>T	NP_001313232.1:p.Asn529Tyr
NM_001326304.1:c.1297A>T	NP_001313233.1:p.Asn433Tyr
NM_001326305.1:c.1618A>T	NP_001313234.1:p.Asn540Tyr
NM_001326306.1:c.1531A>T	NP_001313235.1:p.Asn511Tyr
NM_001326307.1:c.2083A>T	NP_001313236.1:p.Asn695Tyr
NM_001326308.1:c.1300A>T	NP_001313237.1:p.Asn434Tyr
NM_001326309.1:c.1225A>T	NP_001313238.1:p.Asn409Tyr
NM_001326310.1:c.2143A>T	NP_001313239.1:p.Asn715Tyr
NM_001326311.1:c.1222A>T	NP_001313240.1:p.Asn408Tyr
NM_001326312.1:c.2068A>T	NP_001313241.1:p.Asn690Tyr
NM_001326313.1:c.1534A>T	NP_001313242.1:p.Asn512Tyr
NM_001326314.1:c.1615A>T	NP_001313243.1:p.Asn539Tyr
NM_001326315.1:c.2053A>T	NP_001313244.1:p.Asn685Tyr
NM_001326316.1:c.2053A>T	NP_001313245.1:p.Asn685Tyr
NR_136936.1:n.2223A>T
XM_005268070.5:c.1762A>T	XP_005268127.1:p.Asn588Tyr
XM_005268073.4:c.1264A>T	XP_005268130.1:p.Asn422Tyr
XM_006720257.3:c.1189A>T	XP_006720320.1:p.Asn397Tyr
XM_011537161.3:c.2002A>T	XP_011535463.1:p.Asn668Tyr
XM_024449713.1:c.1186A>T	XP_024305481.1:p.Asn396Tyr
NM_024824.5:c.2158A>T MANE Select	NP_079100.2:p.Asn720Tyr
NM_001160103.2:c.2155A>T	NP_001153575.1:p.Asn719Tyr
NM_001160104.2:c.2140A>T	NP_001153576.1:p.Asn714Tyr
NM_001326295.2:c.1765A>T	NP_001313224.1:p.Asn589Tyr
NM_001326296.2:c.2080A>T	NP_001313225.1:p.Asn694Tyr
NM_001326297.2:c.2056A>T	NP_001313226.1:p.Asn686Tyr
NM_001326298.2:c.1690A>T	NP_001313227.1:p.Asn564Tyr
NM_001326299.2:c.2065A>T	NP_001313228.1:p.Asn689Tyr
NM_001326300.2:c.1693A>T	NP_001313229.1:p.Asn565Tyr
NM_001326301.2:c.1981A>T	NP_001313230.1:p.Asn661Tyr
NM_001326302.2:c.1690A>T	NP_001313231.1:p.Asn564Tyr
NM_001326303.2:c.1585A>T	NP_001313232.1:p.Asn529Tyr
NM_001326304.2:c.1297A>T	NP_001313233.1:p.Asn433Tyr
NM_001326305.2:c.1618A>T	NP_001313234.1:p.Asn540Tyr
NM_001326306.2:c.1531A>T	NP_001313235.1:p.Asn511Tyr
NM_001326307.2:c.2083A>T	NP_001313236.1:p.Asn695Tyr
NM_001326308.2:c.1300A>T	NP_001313237.1:p.Asn434Tyr
NM_001326309.2:c.1225A>T	NP_001313238.1:p.Asn409Tyr
NM_001326310.2:c.2143A>T	NP_001313239.1:p.Asn715Tyr
NM_001326311.2:c.1222A>T	NP_001313240.1:p.Asn408Tyr
NM_001326312.2:c.2068A>T	NP_001313241.1:p.Asn690Tyr
NM_001326313.2:c.1534A>T	NP_001313242.1:p.Asn512Tyr
NM_001326314.2:c.1615A>T	NP_001313243.1:p.Asn539Tyr
NM_001326315.2:c.2053A>T	NP_001313244.1:p.Asn685Tyr
NM_207660.4:c.1687A>T	NP_997543.1:p.Asn563Tyr
NM_207662.4:c.868A>T	NP_997545.2:p.Asn290Tyr
NR_136936.2:n.2095A>T
NM_001326316.2:c.2053A>T	NP_001313245.1:p.Asn685Tyr
NM_207661.3:c.1663A>T	NP_997544.1:p.Asn555Tyr