Canonical Allele Identifier: CA390566010

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077223T>G (hg19) ; chr14:g.88610879T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610879T>G , CM000676.2:g.88610879T>G	GRCh38
NC_000014.8:g.89077223T>G , CM000676.1:g.89077223T>G	GRCh37
NC_000014.7:g.88146976T>G	NCBI36
NG_050601.1:g.52971T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2143T>G MANE Select	ENSP00000251038.5:p.Tyr715Asp
ENST00000649731.1:c.*1351T>G	ENSP00000497757.1:n.*1351T>G
ENST00000251038.9:c.2143T>G	ENSP00000251038.5:p.Tyr715Asp
ENST00000302216.12:c.1672T>G	ENSP00000307025.8:p.Tyr558Asp
ENST00000318308.10:c.853T>G	ENSP00000327176.6:p.Tyr285Asp
ENST00000336693.8:c.1648T>G	ENSP00000338002.4:p.Tyr550Asp
ENST00000393514.9:c.2068T>G	ENSP00000377150.5:p.Tyr690Asp
ENST00000406216.7:c.781T>G	ENSP00000384682.3:p.Tyr261Asp
ENST00000554020.5:n.986T>G
ENST00000555755.5:c.2125T>G	ENSP00000452475.1:p.Tyr709Asp
ENST00000555792.1:c.388T>G	ENSP00000450823.1:p.Tyr130Asp
ENST00000555851.6:n.302T>G
ENST00000555900.5:c.1249T>G	ENSP00000451530.1:p.Tyr417Asp
ENST00000556000.5:c.1887T>G
ENST00000556945.5:c.1750T>G	ENSP00000450474.1:p.Tyr584Asp
ENST00000557491.1:n.1428T>G
ENST00000557607.5:c.1195T>G	ENSP00000452370.1:p.Tyr399Asp
NM_001160103.1:c.2140T>G	NP_001153575.1:p.Tyr714Asp
NM_001160104.1:c.2125T>G	NP_001153576.1:p.Tyr709Asp
NM_024824.4:c.2143T>G	NP_079100.2:p.Tyr715Asp
NM_207660.3:c.1672T>G	NP_997543.1:p.Tyr558Asp
NM_207661.2:c.1648T>G	NP_997544.1:p.Tyr550Asp
NM_207662.3:c.853T>G	NP_997545.2:p.Tyr285Asp
XM_005268067.3:c.2128T>G	XP_005268124.1:p.Tyr710Asp
XM_005268068.3:c.2068T>G	XP_005268125.1:p.Tyr690Asp
XM_005268069.3:c.1750T>G	XP_005268126.1:p.Tyr584Asp
XM_005268070.3:c.1747T>G	XP_005268127.1:p.Tyr583Asp
XM_005268071.3:c.1675T>G	XP_005268128.1:p.Tyr559Asp
XM_005268073.3:c.1249T>G	XP_005268130.1:p.Tyr417Asp
XM_006720257.2:c.1174T>G	XP_006720320.1:p.Tyr392Asp
XM_011537160.1:c.2041T>G	XP_011535462.1:p.Tyr681Asp
XM_011537161.1:c.1987T>G	XP_011535463.1:p.Tyr663Asp
NM_001326295.1:c.1750T>G	NP_001313224.1:p.Tyr584Asp
NM_001326296.1:c.2065T>G	NP_001313225.1:p.Tyr689Asp
NM_001326297.1:c.2041T>G	NP_001313226.1:p.Tyr681Asp
NM_001326298.1:c.1675T>G	NP_001313227.1:p.Tyr559Asp
NM_001326299.1:c.2050T>G	NP_001313228.1:p.Tyr684Asp
NM_001326300.1:c.1678T>G	NP_001313229.1:p.Tyr560Asp
NM_001326301.1:c.1966T>G	NP_001313230.1:p.Tyr656Asp
NM_001326302.1:c.1675T>G	NP_001313231.1:p.Tyr559Asp
NM_001326303.1:c.1570T>G	NP_001313232.1:p.Tyr524Asp
NM_001326304.1:c.1282T>G	NP_001313233.1:p.Tyr428Asp
NM_001326305.1:c.1603T>G	NP_001313234.1:p.Tyr535Asp
NM_001326306.1:c.1516T>G	NP_001313235.1:p.Tyr506Asp
NM_001326307.1:c.2068T>G	NP_001313236.1:p.Tyr690Asp
NM_001326308.1:c.1285T>G	NP_001313237.1:p.Tyr429Asp
NM_001326309.1:c.1210T>G	NP_001313238.1:p.Tyr404Asp
NM_001326310.1:c.2128T>G	NP_001313239.1:p.Tyr710Asp
NM_001326311.1:c.1207T>G	NP_001313240.1:p.Tyr403Asp
NM_001326312.1:c.2053T>G	NP_001313241.1:p.Tyr685Asp
NM_001326313.1:c.1519T>G	NP_001313242.1:p.Tyr507Asp
NM_001326314.1:c.1600T>G	NP_001313243.1:p.Tyr534Asp
NM_001326315.1:c.2038T>G	NP_001313244.1:p.Tyr680Asp
NM_001326316.1:c.2038T>G	NP_001313245.1:p.Tyr680Asp
NR_136936.1:n.2208T>G
XM_005268070.5:c.1747T>G	XP_005268127.1:p.Tyr583Asp
XM_005268073.4:c.1249T>G	XP_005268130.1:p.Tyr417Asp
XM_006720257.3:c.1174T>G	XP_006720320.1:p.Tyr392Asp
XM_011537161.3:c.1987T>G	XP_011535463.1:p.Tyr663Asp
XM_024449713.1:c.1171T>G	XP_024305481.1:p.Tyr391Asp
NM_024824.5:c.2143T>G MANE Select	NP_079100.2:p.Tyr715Asp
NM_001160103.2:c.2140T>G	NP_001153575.1:p.Tyr714Asp
NM_001160104.2:c.2125T>G	NP_001153576.1:p.Tyr709Asp
NM_001326295.2:c.1750T>G	NP_001313224.1:p.Tyr584Asp
NM_001326296.2:c.2065T>G	NP_001313225.1:p.Tyr689Asp
NM_001326297.2:c.2041T>G	NP_001313226.1:p.Tyr681Asp
NM_001326298.2:c.1675T>G	NP_001313227.1:p.Tyr559Asp
NM_001326299.2:c.2050T>G	NP_001313228.1:p.Tyr684Asp
NM_001326300.2:c.1678T>G	NP_001313229.1:p.Tyr560Asp
NM_001326301.2:c.1966T>G	NP_001313230.1:p.Tyr656Asp
NM_001326302.2:c.1675T>G	NP_001313231.1:p.Tyr559Asp
NM_001326303.2:c.1570T>G	NP_001313232.1:p.Tyr524Asp
NM_001326304.2:c.1282T>G	NP_001313233.1:p.Tyr428Asp
NM_001326305.2:c.1603T>G	NP_001313234.1:p.Tyr535Asp
NM_001326306.2:c.1516T>G	NP_001313235.1:p.Tyr506Asp
NM_001326307.2:c.2068T>G	NP_001313236.1:p.Tyr690Asp
NM_001326308.2:c.1285T>G	NP_001313237.1:p.Tyr429Asp
NM_001326309.2:c.1210T>G	NP_001313238.1:p.Tyr404Asp
NM_001326310.2:c.2128T>G	NP_001313239.1:p.Tyr710Asp
NM_001326311.2:c.1207T>G	NP_001313240.1:p.Tyr403Asp
NM_001326312.2:c.2053T>G	NP_001313241.1:p.Tyr685Asp
NM_001326313.2:c.1519T>G	NP_001313242.1:p.Tyr507Asp
NM_001326314.2:c.1600T>G	NP_001313243.1:p.Tyr534Asp
NM_001326315.2:c.2038T>G	NP_001313244.1:p.Tyr680Asp
NM_207660.4:c.1672T>G	NP_997543.1:p.Tyr558Asp
NM_207662.4:c.853T>G	NP_997545.2:p.Tyr285Asp
NR_136936.2:n.2080T>G
NM_001326316.2:c.2038T>G	NP_001313245.1:p.Tyr680Asp
NM_207661.3:c.1648T>G	NP_997544.1:p.Tyr550Asp