Canonical Allele Identifier: CA390565983

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077221T>C (hg19) ; chr14:g.88610877T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610877T>C , CM000676.2:g.88610877T>C	GRCh38
NC_000014.8:g.89077221T>C , CM000676.1:g.89077221T>C	GRCh37
NC_000014.7:g.88146974T>C	NCBI36
NG_050601.1:g.52969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2141T>C MANE Select	ENSP00000251038.5:p.Phe714Ser
ENST00000649731.1:c.*1349T>C	ENSP00000497757.1:n.*1349T>C
ENST00000251038.9:c.2141T>C	ENSP00000251038.5:p.Phe714Ser
ENST00000302216.12:c.1670T>C	ENSP00000307025.8:p.Phe557Ser
ENST00000318308.10:c.851T>C	ENSP00000327176.6:p.Phe284Ser
ENST00000336693.8:c.1646T>C	ENSP00000338002.4:p.Phe549Ser
ENST00000393514.9:c.2066T>C	ENSP00000377150.5:p.Phe689Ser
ENST00000406216.7:c.779T>C	ENSP00000384682.3:p.Phe260Ser
ENST00000554020.5:n.984T>C
ENST00000555755.5:c.2123T>C	ENSP00000452475.1:p.Phe708Ser
ENST00000555792.1:c.386T>C	ENSP00000450823.1:p.Phe129Ser
ENST00000555851.6:n.300T>C
ENST00000555900.5:c.1247T>C	ENSP00000451530.1:p.Phe416Ser
ENST00000556000.5:c.1885T>C
ENST00000556945.5:c.1748T>C	ENSP00000450474.1:p.Phe583Ser
ENST00000557491.1:n.1426T>C
ENST00000557607.5:c.1193T>C	ENSP00000452370.1:p.Phe398Ser
NM_001160103.1:c.2138T>C	NP_001153575.1:p.Phe713Ser
NM_001160104.1:c.2123T>C	NP_001153576.1:p.Phe708Ser
NM_024824.4:c.2141T>C	NP_079100.2:p.Phe714Ser
NM_207660.3:c.1670T>C	NP_997543.1:p.Phe557Ser
NM_207661.2:c.1646T>C	NP_997544.1:p.Phe549Ser
NM_207662.3:c.851T>C	NP_997545.2:p.Phe284Ser
XM_005268067.3:c.2126T>C	XP_005268124.1:p.Phe709Ser
XM_005268068.3:c.2066T>C	XP_005268125.1:p.Phe689Ser
XM_005268069.3:c.1748T>C	XP_005268126.1:p.Phe583Ser
XM_005268070.3:c.1745T>C	XP_005268127.1:p.Phe582Ser
XM_005268071.3:c.1673T>C	XP_005268128.1:p.Phe558Ser
XM_005268073.3:c.1247T>C	XP_005268130.1:p.Phe416Ser
XM_006720257.2:c.1172T>C	XP_006720320.1:p.Phe391Ser
XM_011537160.1:c.2039T>C	XP_011535462.1:p.Phe680Ser
XM_011537161.1:c.1985T>C	XP_011535463.1:p.Phe662Ser
NM_001326295.1:c.1748T>C	NP_001313224.1:p.Phe583Ser
NM_001326296.1:c.2063T>C	NP_001313225.1:p.Phe688Ser
NM_001326297.1:c.2039T>C	NP_001313226.1:p.Phe680Ser
NM_001326298.1:c.1673T>C	NP_001313227.1:p.Phe558Ser
NM_001326299.1:c.2048T>C	NP_001313228.1:p.Phe683Ser
NM_001326300.1:c.1676T>C	NP_001313229.1:p.Phe559Ser
NM_001326301.1:c.1964T>C	NP_001313230.1:p.Phe655Ser
NM_001326302.1:c.1673T>C	NP_001313231.1:p.Phe558Ser
NM_001326303.1:c.1568T>C	NP_001313232.1:p.Phe523Ser
NM_001326304.1:c.1280T>C	NP_001313233.1:p.Phe427Ser
NM_001326305.1:c.1601T>C	NP_001313234.1:p.Phe534Ser
NM_001326306.1:c.1514T>C	NP_001313235.1:p.Phe505Ser
NM_001326307.1:c.2066T>C	NP_001313236.1:p.Phe689Ser
NM_001326308.1:c.1283T>C	NP_001313237.1:p.Phe428Ser
NM_001326309.1:c.1208T>C	NP_001313238.1:p.Phe403Ser
NM_001326310.1:c.2126T>C	NP_001313239.1:p.Phe709Ser
NM_001326311.1:c.1205T>C	NP_001313240.1:p.Phe402Ser
NM_001326312.1:c.2051T>C	NP_001313241.1:p.Phe684Ser
NM_001326313.1:c.1517T>C	NP_001313242.1:p.Phe506Ser
NM_001326314.1:c.1598T>C	NP_001313243.1:p.Phe533Ser
NM_001326315.1:c.2036T>C	NP_001313244.1:p.Phe679Ser
NM_001326316.1:c.2036T>C	NP_001313245.1:p.Phe679Ser
NR_136936.1:n.2206T>C
XM_005268070.5:c.1745T>C	XP_005268127.1:p.Phe582Ser
XM_005268073.4:c.1247T>C	XP_005268130.1:p.Phe416Ser
XM_006720257.3:c.1172T>C	XP_006720320.1:p.Phe391Ser
XM_011537161.3:c.1985T>C	XP_011535463.1:p.Phe662Ser
XM_024449713.1:c.1169T>C	XP_024305481.1:p.Phe390Ser
NM_024824.5:c.2141T>C MANE Select	NP_079100.2:p.Phe714Ser
NM_001160103.2:c.2138T>C	NP_001153575.1:p.Phe713Ser
NM_001160104.2:c.2123T>C	NP_001153576.1:p.Phe708Ser
NM_001326295.2:c.1748T>C	NP_001313224.1:p.Phe583Ser
NM_001326296.2:c.2063T>C	NP_001313225.1:p.Phe688Ser
NM_001326297.2:c.2039T>C	NP_001313226.1:p.Phe680Ser
NM_001326298.2:c.1673T>C	NP_001313227.1:p.Phe558Ser
NM_001326299.2:c.2048T>C	NP_001313228.1:p.Phe683Ser
NM_001326300.2:c.1676T>C	NP_001313229.1:p.Phe559Ser
NM_001326301.2:c.1964T>C	NP_001313230.1:p.Phe655Ser
NM_001326302.2:c.1673T>C	NP_001313231.1:p.Phe558Ser
NM_001326303.2:c.1568T>C	NP_001313232.1:p.Phe523Ser
NM_001326304.2:c.1280T>C	NP_001313233.1:p.Phe427Ser
NM_001326305.2:c.1601T>C	NP_001313234.1:p.Phe534Ser
NM_001326306.2:c.1514T>C	NP_001313235.1:p.Phe505Ser
NM_001326307.2:c.2066T>C	NP_001313236.1:p.Phe689Ser
NM_001326308.2:c.1283T>C	NP_001313237.1:p.Phe428Ser
NM_001326309.2:c.1208T>C	NP_001313238.1:p.Phe403Ser
NM_001326310.2:c.2126T>C	NP_001313239.1:p.Phe709Ser
NM_001326311.2:c.1205T>C	NP_001313240.1:p.Phe402Ser
NM_001326312.2:c.2051T>C	NP_001313241.1:p.Phe684Ser
NM_001326313.2:c.1517T>C	NP_001313242.1:p.Phe506Ser
NM_001326314.2:c.1598T>C	NP_001313243.1:p.Phe533Ser
NM_001326315.2:c.2036T>C	NP_001313244.1:p.Phe679Ser
NM_207660.4:c.1670T>C	NP_997543.1:p.Phe557Ser
NM_207662.4:c.851T>C	NP_997545.2:p.Phe284Ser
NR_136936.2:n.2078T>C
NM_001326316.2:c.2036T>C	NP_001313245.1:p.Phe679Ser
NM_207661.3:c.1646T>C	NP_997544.1:p.Phe549Ser