Canonical Allele Identifier: CA487280462

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077273A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610929A>C , CM000676.2:g.88610929A>C	GRCh38
NC_000014.8:g.89077273A>C , CM000676.1:g.89077273A>C	GRCh37
NC_000014.7:g.88147026A>C	NCBI36
NG_050601.1:g.53021A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2193A>C MANE Select	ENSP00000251038.5:p.Arg731=
ENST00000649731.1:c.*1401A>C	ENSP00000497757.1:n.*1401A>C
ENST00000251038.9:c.2193A>C	ENSP00000251038.5:p.Arg731=
ENST00000302216.12:c.1722A>C	ENSP00000307025.8:p.Arg574=
ENST00000318308.10:c.903A>C	ENSP00000327176.6:p.Arg301=
ENST00000336693.8:c.1698A>C	ENSP00000338002.4:p.Arg566=
ENST00000393514.9:c.2118A>C	ENSP00000377150.5:p.Arg706=
ENST00000406216.7:c.831A>C	ENSP00000384682.3:p.Arg277=
ENST00000554020.5:n.1036A>C
ENST00000555755.5:c.2175A>C	ENSP00000452475.1:p.Arg725=
ENST00000555792.1:c.438A>C	ENSP00000450823.1:p.Arg146=
ENST00000555851.6:n.352A>C
ENST00000555900.5:c.1299A>C	ENSP00000451530.1:p.Arg433=
ENST00000556000.5:c.1937A>C
ENST00000556945.5:c.1800A>C	ENSP00000450474.1:p.Arg600=
ENST00000557491.1:n.1478A>C
ENST00000557607.5:c.1245A>C	ENSP00000452370.1:p.Arg415=
NM_001160103.1:c.2190A>C	NP_001153575.1:p.Arg730=
NM_001160104.1:c.2175A>C	NP_001153576.1:p.Arg725=
NM_024824.4:c.2193A>C	NP_079100.2:p.Arg731=
NM_207660.3:c.1722A>C	NP_997543.1:p.Arg574=
NM_207661.2:c.1698A>C	NP_997544.1:p.Arg566=
NM_207662.3:c.903A>C	NP_997545.2:p.Arg301=
XM_005268067.3:c.2178A>C	XP_005268124.1:p.Arg726=
XM_005268068.3:c.2118A>C	XP_005268125.1:p.Arg706=
XM_005268069.3:c.1800A>C	XP_005268126.1:p.Arg600=
XM_005268070.3:c.1797A>C	XP_005268127.1:p.Arg599=
XM_005268071.3:c.1725A>C	XP_005268128.1:p.Arg575=
XM_005268073.3:c.1299A>C	XP_005268130.1:p.Arg433=
XM_006720257.2:c.1224A>C	XP_006720320.1:p.Arg408=
XM_011537160.1:c.2091A>C	XP_011535462.1:p.Arg697=
XM_011537161.1:c.2037A>C	XP_011535463.1:p.Arg679=
NM_001326295.1:c.1800A>C	NP_001313224.1:p.Arg600=
NM_001326296.1:c.2115A>C	NP_001313225.1:p.Arg705=
NM_001326297.1:c.2091A>C	NP_001313226.1:p.Arg697=
NM_001326298.1:c.1725A>C	NP_001313227.1:p.Arg575=
NM_001326299.1:c.2100A>C	NP_001313228.1:p.Arg700=
NM_001326300.1:c.1728A>C	NP_001313229.1:p.Arg576=
NM_001326301.1:c.2016A>C	NP_001313230.1:p.Arg672=
NM_001326302.1:c.1725A>C	NP_001313231.1:p.Arg575=
NM_001326303.1:c.1620A>C	NP_001313232.1:p.Arg540=
NM_001326304.1:c.1332A>C	NP_001313233.1:p.Arg444=
NM_001326305.1:c.1653A>C	NP_001313234.1:p.Arg551=
NM_001326306.1:c.1566A>C	NP_001313235.1:p.Arg522=
NM_001326307.1:c.2118A>C	NP_001313236.1:p.Arg706=
NM_001326308.1:c.1335A>C	NP_001313237.1:p.Arg445=
NM_001326309.1:c.1260A>C	NP_001313238.1:p.Arg420=
NM_001326310.1:c.2178A>C	NP_001313239.1:p.Arg726=
NM_001326311.1:c.1257A>C	NP_001313240.1:p.Arg419=
NM_001326312.1:c.2103A>C	NP_001313241.1:p.Arg701=
NM_001326313.1:c.1569A>C	NP_001313242.1:p.Arg523=
NM_001326314.1:c.1650A>C	NP_001313243.1:p.Arg550=
NM_001326315.1:c.2088A>C	NP_001313244.1:p.Arg696=
NM_001326316.1:c.2088A>C	NP_001313245.1:p.Arg696=
NR_136936.1:n.2258A>C
XM_005268070.5:c.1797A>C	XP_005268127.1:p.Arg599=
XM_005268073.4:c.1299A>C	XP_005268130.1:p.Arg433=
XM_006720257.3:c.1224A>C	XP_006720320.1:p.Arg408=
XM_011537161.3:c.2037A>C	XP_011535463.1:p.Arg679=
XM_024449713.1:c.1221A>C	XP_024305481.1:p.Arg407=
NM_024824.5:c.2193A>C MANE Select	NP_079100.2:p.Arg731=
NM_001160103.2:c.2190A>C	NP_001153575.1:p.Arg730=
NM_001160104.2:c.2175A>C	NP_001153576.1:p.Arg725=
NM_001326295.2:c.1800A>C	NP_001313224.1:p.Arg600=
NM_001326296.2:c.2115A>C	NP_001313225.1:p.Arg705=
NM_001326297.2:c.2091A>C	NP_001313226.1:p.Arg697=
NM_001326298.2:c.1725A>C	NP_001313227.1:p.Arg575=
NM_001326299.2:c.2100A>C	NP_001313228.1:p.Arg700=
NM_001326300.2:c.1728A>C	NP_001313229.1:p.Arg576=
NM_001326301.2:c.2016A>C	NP_001313230.1:p.Arg672=
NM_001326302.2:c.1725A>C	NP_001313231.1:p.Arg575=
NM_001326303.2:c.1620A>C	NP_001313232.1:p.Arg540=
NM_001326304.2:c.1332A>C	NP_001313233.1:p.Arg444=
NM_001326305.2:c.1653A>C	NP_001313234.1:p.Arg551=
NM_001326306.2:c.1566A>C	NP_001313235.1:p.Arg522=
NM_001326307.2:c.2118A>C	NP_001313236.1:p.Arg706=
NM_001326308.2:c.1335A>C	NP_001313237.1:p.Arg445=
NM_001326309.2:c.1260A>C	NP_001313238.1:p.Arg420=
NM_001326310.2:c.2178A>C	NP_001313239.1:p.Arg726=
NM_001326311.2:c.1257A>C	NP_001313240.1:p.Arg419=
NM_001326312.2:c.2103A>C	NP_001313241.1:p.Arg701=
NM_001326313.2:c.1569A>C	NP_001313242.1:p.Arg523=
NM_001326314.2:c.1650A>C	NP_001313243.1:p.Arg550=
NM_001326315.2:c.2088A>C	NP_001313244.1:p.Arg696=
NM_207660.4:c.1722A>C	NP_997543.1:p.Arg574=
NM_207662.4:c.903A>C	NP_997545.2:p.Arg301=
NR_136936.2:n.2130A>C
NM_001326316.2:c.2088A>C	NP_001313245.1:p.Arg696=
NM_207661.3:c.1698A>C	NP_997544.1:p.Arg566=