Canonical Allele Identifier: CA487280426

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077219A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610875A>C , CM000676.2:g.88610875A>C	GRCh38
NC_000014.8:g.89077219A>C , CM000676.1:g.89077219A>C	GRCh37
NC_000014.7:g.88146972A>C	NCBI36
NG_050601.1:g.52967A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2139A>C MANE Select	ENSP00000251038.5:p.Thr713=
ENST00000649731.1:c.*1347A>C	ENSP00000497757.1:n.*1347A>C
ENST00000251038.9:c.2139A>C	ENSP00000251038.5:p.Thr713=
ENST00000302216.12:c.1668A>C	ENSP00000307025.8:p.Thr556=
ENST00000318308.10:c.849A>C	ENSP00000327176.6:p.Thr283=
ENST00000336693.8:c.1644A>C	ENSP00000338002.4:p.Thr548=
ENST00000393514.9:c.2064A>C	ENSP00000377150.5:p.Thr688=
ENST00000406216.7:c.777A>C	ENSP00000384682.3:p.Thr259=
ENST00000554020.5:n.982A>C
ENST00000555755.5:c.2121A>C	ENSP00000452475.1:p.Thr707=
ENST00000555792.1:c.384A>C	ENSP00000450823.1:p.Thr128=
ENST00000555851.6:n.298A>C
ENST00000555900.5:c.1245A>C	ENSP00000451530.1:p.Thr415=
ENST00000556000.5:c.1883A>C
ENST00000556945.5:c.1746A>C	ENSP00000450474.1:p.Thr582=
ENST00000557491.1:n.1424A>C
ENST00000557607.5:c.1191A>C	ENSP00000452370.1:p.Thr397=
NM_001160103.1:c.2136A>C	NP_001153575.1:p.Thr712=
NM_001160104.1:c.2121A>C	NP_001153576.1:p.Thr707=
NM_024824.4:c.2139A>C	NP_079100.2:p.Thr713=
NM_207660.3:c.1668A>C	NP_997543.1:p.Thr556=
NM_207661.2:c.1644A>C	NP_997544.1:p.Thr548=
NM_207662.3:c.849A>C	NP_997545.2:p.Thr283=
XM_005268067.3:c.2124A>C	XP_005268124.1:p.Thr708=
XM_005268068.3:c.2064A>C	XP_005268125.1:p.Thr688=
XM_005268069.3:c.1746A>C	XP_005268126.1:p.Thr582=
XM_005268070.3:c.1743A>C	XP_005268127.1:p.Thr581=
XM_005268071.3:c.1671A>C	XP_005268128.1:p.Thr557=
XM_005268073.3:c.1245A>C	XP_005268130.1:p.Thr415=
XM_006720257.2:c.1170A>C	XP_006720320.1:p.Thr390=
XM_011537160.1:c.2037A>C	XP_011535462.1:p.Thr679=
XM_011537161.1:c.1983A>C	XP_011535463.1:p.Thr661=
NM_001326295.1:c.1746A>C	NP_001313224.1:p.Thr582=
NM_001326296.1:c.2061A>C	NP_001313225.1:p.Thr687=
NM_001326297.1:c.2037A>C	NP_001313226.1:p.Thr679=
NM_001326298.1:c.1671A>C	NP_001313227.1:p.Thr557=
NM_001326299.1:c.2046A>C	NP_001313228.1:p.Thr682=
NM_001326300.1:c.1674A>C	NP_001313229.1:p.Thr558=
NM_001326301.1:c.1962A>C	NP_001313230.1:p.Thr654=
NM_001326302.1:c.1671A>C	NP_001313231.1:p.Thr557=
NM_001326303.1:c.1566A>C	NP_001313232.1:p.Thr522=
NM_001326304.1:c.1278A>C	NP_001313233.1:p.Thr426=
NM_001326305.1:c.1599A>C	NP_001313234.1:p.Thr533=
NM_001326306.1:c.1512A>C	NP_001313235.1:p.Thr504=
NM_001326307.1:c.2064A>C	NP_001313236.1:p.Thr688=
NM_001326308.1:c.1281A>C	NP_001313237.1:p.Thr427=
NM_001326309.1:c.1206A>C	NP_001313238.1:p.Thr402=
NM_001326310.1:c.2124A>C	NP_001313239.1:p.Thr708=
NM_001326311.1:c.1203A>C	NP_001313240.1:p.Thr401=
NM_001326312.1:c.2049A>C	NP_001313241.1:p.Thr683=
NM_001326313.1:c.1515A>C	NP_001313242.1:p.Thr505=
NM_001326314.1:c.1596A>C	NP_001313243.1:p.Thr532=
NM_001326315.1:c.2034A>C	NP_001313244.1:p.Thr678=
NM_001326316.1:c.2034A>C	NP_001313245.1:p.Thr678=
NR_136936.1:n.2204A>C
XM_005268070.5:c.1743A>C	XP_005268127.1:p.Thr581=
XM_005268073.4:c.1245A>C	XP_005268130.1:p.Thr415=
XM_006720257.3:c.1170A>C	XP_006720320.1:p.Thr390=
XM_011537161.3:c.1983A>C	XP_011535463.1:p.Thr661=
XM_024449713.1:c.1167A>C	XP_024305481.1:p.Thr389=
NM_024824.5:c.2139A>C MANE Select	NP_079100.2:p.Thr713=
NM_001160103.2:c.2136A>C	NP_001153575.1:p.Thr712=
NM_001160104.2:c.2121A>C	NP_001153576.1:p.Thr707=
NM_001326295.2:c.1746A>C	NP_001313224.1:p.Thr582=
NM_001326296.2:c.2061A>C	NP_001313225.1:p.Thr687=
NM_001326297.2:c.2037A>C	NP_001313226.1:p.Thr679=
NM_001326298.2:c.1671A>C	NP_001313227.1:p.Thr557=
NM_001326299.2:c.2046A>C	NP_001313228.1:p.Thr682=
NM_001326300.2:c.1674A>C	NP_001313229.1:p.Thr558=
NM_001326301.2:c.1962A>C	NP_001313230.1:p.Thr654=
NM_001326302.2:c.1671A>C	NP_001313231.1:p.Thr557=
NM_001326303.2:c.1566A>C	NP_001313232.1:p.Thr522=
NM_001326304.2:c.1278A>C	NP_001313233.1:p.Thr426=
NM_001326305.2:c.1599A>C	NP_001313234.1:p.Thr533=
NM_001326306.2:c.1512A>C	NP_001313235.1:p.Thr504=
NM_001326307.2:c.2064A>C	NP_001313236.1:p.Thr688=
NM_001326308.2:c.1281A>C	NP_001313237.1:p.Thr427=
NM_001326309.2:c.1206A>C	NP_001313238.1:p.Thr402=
NM_001326310.2:c.2124A>C	NP_001313239.1:p.Thr708=
NM_001326311.2:c.1203A>C	NP_001313240.1:p.Thr401=
NM_001326312.2:c.2049A>C	NP_001313241.1:p.Thr683=
NM_001326313.2:c.1515A>C	NP_001313242.1:p.Thr505=
NM_001326314.2:c.1596A>C	NP_001313243.1:p.Thr532=
NM_001326315.2:c.2034A>C	NP_001313244.1:p.Thr678=
NM_207660.4:c.1668A>C	NP_997543.1:p.Thr556=
NM_207662.4:c.849A>C	NP_997545.2:p.Thr283=
NR_136936.2:n.2076A>C
NM_001326316.2:c.2034A>C	NP_001313245.1:p.Thr678=
NM_207661.3:c.1644A>C	NP_997544.1:p.Thr548=