Canonical Allele Identifier: CA390565887

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077212A>T (hg19) ; chr14:g.88610868A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610868A>T , CM000676.2:g.88610868A>T	GRCh38
NC_000014.8:g.89077212A>T , CM000676.1:g.89077212A>T	GRCh37
NC_000014.7:g.88146965A>T	NCBI36
NG_050601.1:g.52960A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2132A>T MANE Select	ENSP00000251038.5:p.Asp711Val
ENST00000649731.1:c.*1340A>T	ENSP00000497757.1:n.*1340A>T
ENST00000251038.9:c.2132A>T	ENSP00000251038.5:p.Asp711Val
ENST00000302216.12:c.1661A>T	ENSP00000307025.8:p.Asp554Val
ENST00000318308.10:c.842A>T	ENSP00000327176.6:p.Asp281Val
ENST00000336693.8:c.1637A>T	ENSP00000338002.4:p.Asp546Val
ENST00000393514.9:c.2057A>T	ENSP00000377150.5:p.Asp686Val
ENST00000406216.7:c.770A>T	ENSP00000384682.3:p.Asp257Val
ENST00000554020.5:n.975A>T
ENST00000555755.5:c.2114A>T	ENSP00000452475.1:p.Asp705Val
ENST00000555792.1:c.377A>T	ENSP00000450823.1:p.Asp126Val
ENST00000555851.6:n.291A>T
ENST00000555900.5:c.1238A>T	ENSP00000451530.1:p.Asp413Val
ENST00000556000.5:c.1876A>T
ENST00000556945.5:c.1739A>T	ENSP00000450474.1:p.Asp580Val
ENST00000557491.1:n.1417A>T
ENST00000557607.5:c.1184A>T	ENSP00000452370.1:p.Asp395Val
NM_001160103.1:c.2129A>T	NP_001153575.1:p.Asp710Val
NM_001160104.1:c.2114A>T	NP_001153576.1:p.Asp705Val
NM_024824.4:c.2132A>T	NP_079100.2:p.Asp711Val
NM_207660.3:c.1661A>T	NP_997543.1:p.Asp554Val
NM_207661.2:c.1637A>T	NP_997544.1:p.Asp546Val
NM_207662.3:c.842A>T	NP_997545.2:p.Asp281Val
XM_005268067.3:c.2117A>T	XP_005268124.1:p.Asp706Val
XM_005268068.3:c.2057A>T	XP_005268125.1:p.Asp686Val
XM_005268069.3:c.1739A>T	XP_005268126.1:p.Asp580Val
XM_005268070.3:c.1736A>T	XP_005268127.1:p.Asp579Val
XM_005268071.3:c.1664A>T	XP_005268128.1:p.Asp555Val
XM_005268073.3:c.1238A>T	XP_005268130.1:p.Asp413Val
XM_006720257.2:c.1163A>T	XP_006720320.1:p.Asp388Val
XM_011537160.1:c.2030A>T	XP_011535462.1:p.Asp677Val
XM_011537161.1:c.1976A>T	XP_011535463.1:p.Asp659Val
NM_001326295.1:c.1739A>T	NP_001313224.1:p.Asp580Val
NM_001326296.1:c.2054A>T	NP_001313225.1:p.Asp685Val
NM_001326297.1:c.2030A>T	NP_001313226.1:p.Asp677Val
NM_001326298.1:c.1664A>T	NP_001313227.1:p.Asp555Val
NM_001326299.1:c.2039A>T	NP_001313228.1:p.Asp680Val
NM_001326300.1:c.1667A>T	NP_001313229.1:p.Asp556Val
NM_001326301.1:c.1955A>T	NP_001313230.1:p.Asp652Val
NM_001326302.1:c.1664A>T	NP_001313231.1:p.Asp555Val
NM_001326303.1:c.1559A>T	NP_001313232.1:p.Asp520Val
NM_001326304.1:c.1271A>T	NP_001313233.1:p.Asp424Val
NM_001326305.1:c.1592A>T	NP_001313234.1:p.Asp531Val
NM_001326306.1:c.1505A>T	NP_001313235.1:p.Asp502Val
NM_001326307.1:c.2057A>T	NP_001313236.1:p.Asp686Val
NM_001326308.1:c.1274A>T	NP_001313237.1:p.Asp425Val
NM_001326309.1:c.1199A>T	NP_001313238.1:p.Asp400Val
NM_001326310.1:c.2117A>T	NP_001313239.1:p.Asp706Val
NM_001326311.1:c.1196A>T	NP_001313240.1:p.Asp399Val
NM_001326312.1:c.2042A>T	NP_001313241.1:p.Asp681Val
NM_001326313.1:c.1508A>T	NP_001313242.1:p.Asp503Val
NM_001326314.1:c.1589A>T	NP_001313243.1:p.Asp530Val
NM_001326315.1:c.2027A>T	NP_001313244.1:p.Asp676Val
NM_001326316.1:c.2027A>T	NP_001313245.1:p.Asp676Val
NR_136936.1:n.2197A>T
XM_005268070.5:c.1736A>T	XP_005268127.1:p.Asp579Val
XM_005268073.4:c.1238A>T	XP_005268130.1:p.Asp413Val
XM_006720257.3:c.1163A>T	XP_006720320.1:p.Asp388Val
XM_011537161.3:c.1976A>T	XP_011535463.1:p.Asp659Val
XM_024449713.1:c.1160A>T	XP_024305481.1:p.Asp387Val
NM_024824.5:c.2132A>T MANE Select	NP_079100.2:p.Asp711Val
NM_001160103.2:c.2129A>T	NP_001153575.1:p.Asp710Val
NM_001160104.2:c.2114A>T	NP_001153576.1:p.Asp705Val
NM_001326295.2:c.1739A>T	NP_001313224.1:p.Asp580Val
NM_001326296.2:c.2054A>T	NP_001313225.1:p.Asp685Val
NM_001326297.2:c.2030A>T	NP_001313226.1:p.Asp677Val
NM_001326298.2:c.1664A>T	NP_001313227.1:p.Asp555Val
NM_001326299.2:c.2039A>T	NP_001313228.1:p.Asp680Val
NM_001326300.2:c.1667A>T	NP_001313229.1:p.Asp556Val
NM_001326301.2:c.1955A>T	NP_001313230.1:p.Asp652Val
NM_001326302.2:c.1664A>T	NP_001313231.1:p.Asp555Val
NM_001326303.2:c.1559A>T	NP_001313232.1:p.Asp520Val
NM_001326304.2:c.1271A>T	NP_001313233.1:p.Asp424Val
NM_001326305.2:c.1592A>T	NP_001313234.1:p.Asp531Val
NM_001326306.2:c.1505A>T	NP_001313235.1:p.Asp502Val
NM_001326307.2:c.2057A>T	NP_001313236.1:p.Asp686Val
NM_001326308.2:c.1274A>T	NP_001313237.1:p.Asp425Val
NM_001326309.2:c.1199A>T	NP_001313238.1:p.Asp400Val
NM_001326310.2:c.2117A>T	NP_001313239.1:p.Asp706Val
NM_001326311.2:c.1196A>T	NP_001313240.1:p.Asp399Val
NM_001326312.2:c.2042A>T	NP_001313241.1:p.Asp681Val
NM_001326313.2:c.1508A>T	NP_001313242.1:p.Asp503Val
NM_001326314.2:c.1589A>T	NP_001313243.1:p.Asp530Val
NM_001326315.2:c.2027A>T	NP_001313244.1:p.Asp676Val
NM_207660.4:c.1661A>T	NP_997543.1:p.Asp554Val
NM_207662.4:c.842A>T	NP_997545.2:p.Asp281Val
NR_136936.2:n.2069A>T
NM_001326316.2:c.2027A>T	NP_001313245.1:p.Asp676Val
NM_207661.3:c.1637A>T	NP_997544.1:p.Asp546Val