Canonical Allele Identifier: CA390566014

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077224A>C (hg19) ; chr14:g.88610880A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610880A>C , CM000676.2:g.88610880A>C	GRCh38
NC_000014.8:g.89077224A>C , CM000676.1:g.89077224A>C	GRCh37
NC_000014.7:g.88146977A>C	NCBI36
NG_050601.1:g.52972A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2144A>C MANE Select	ENSP00000251038.5:p.Tyr715Ser
ENST00000649731.1:c.*1352A>C	ENSP00000497757.1:n.*1352A>C
ENST00000251038.9:c.2144A>C	ENSP00000251038.5:p.Tyr715Ser
ENST00000302216.12:c.1673A>C	ENSP00000307025.8:p.Tyr558Ser
ENST00000318308.10:c.854A>C	ENSP00000327176.6:p.Tyr285Ser
ENST00000336693.8:c.1649A>C	ENSP00000338002.4:p.Tyr550Ser
ENST00000393514.9:c.2069A>C	ENSP00000377150.5:p.Tyr690Ser
ENST00000406216.7:c.782A>C	ENSP00000384682.3:p.Tyr261Ser
ENST00000554020.5:n.987A>C
ENST00000555755.5:c.2126A>C	ENSP00000452475.1:p.Tyr709Ser
ENST00000555792.1:c.389A>C	ENSP00000450823.1:p.Tyr130Ser
ENST00000555851.6:n.303A>C
ENST00000555900.5:c.1250A>C	ENSP00000451530.1:p.Tyr417Ser
ENST00000556000.5:c.1888A>C
ENST00000556945.5:c.1751A>C	ENSP00000450474.1:p.Tyr584Ser
ENST00000557491.1:n.1429A>C
ENST00000557607.5:c.1196A>C	ENSP00000452370.1:p.Tyr399Ser
NM_001160103.1:c.2141A>C	NP_001153575.1:p.Tyr714Ser
NM_001160104.1:c.2126A>C	NP_001153576.1:p.Tyr709Ser
NM_024824.4:c.2144A>C	NP_079100.2:p.Tyr715Ser
NM_207660.3:c.1673A>C	NP_997543.1:p.Tyr558Ser
NM_207661.2:c.1649A>C	NP_997544.1:p.Tyr550Ser
NM_207662.3:c.854A>C	NP_997545.2:p.Tyr285Ser
XM_005268067.3:c.2129A>C	XP_005268124.1:p.Tyr710Ser
XM_005268068.3:c.2069A>C	XP_005268125.1:p.Tyr690Ser
XM_005268069.3:c.1751A>C	XP_005268126.1:p.Tyr584Ser
XM_005268070.3:c.1748A>C	XP_005268127.1:p.Tyr583Ser
XM_005268071.3:c.1676A>C	XP_005268128.1:p.Tyr559Ser
XM_005268073.3:c.1250A>C	XP_005268130.1:p.Tyr417Ser
XM_006720257.2:c.1175A>C	XP_006720320.1:p.Tyr392Ser
XM_011537160.1:c.2042A>C	XP_011535462.1:p.Tyr681Ser
XM_011537161.1:c.1988A>C	XP_011535463.1:p.Tyr663Ser
NM_001326295.1:c.1751A>C	NP_001313224.1:p.Tyr584Ser
NM_001326296.1:c.2066A>C	NP_001313225.1:p.Tyr689Ser
NM_001326297.1:c.2042A>C	NP_001313226.1:p.Tyr681Ser
NM_001326298.1:c.1676A>C	NP_001313227.1:p.Tyr559Ser
NM_001326299.1:c.2051A>C	NP_001313228.1:p.Tyr684Ser
NM_001326300.1:c.1679A>C	NP_001313229.1:p.Tyr560Ser
NM_001326301.1:c.1967A>C	NP_001313230.1:p.Tyr656Ser
NM_001326302.1:c.1676A>C	NP_001313231.1:p.Tyr559Ser
NM_001326303.1:c.1571A>C	NP_001313232.1:p.Tyr524Ser
NM_001326304.1:c.1283A>C	NP_001313233.1:p.Tyr428Ser
NM_001326305.1:c.1604A>C	NP_001313234.1:p.Tyr535Ser
NM_001326306.1:c.1517A>C	NP_001313235.1:p.Tyr506Ser
NM_001326307.1:c.2069A>C	NP_001313236.1:p.Tyr690Ser
NM_001326308.1:c.1286A>C	NP_001313237.1:p.Tyr429Ser
NM_001326309.1:c.1211A>C	NP_001313238.1:p.Tyr404Ser
NM_001326310.1:c.2129A>C	NP_001313239.1:p.Tyr710Ser
NM_001326311.1:c.1208A>C	NP_001313240.1:p.Tyr403Ser
NM_001326312.1:c.2054A>C	NP_001313241.1:p.Tyr685Ser
NM_001326313.1:c.1520A>C	NP_001313242.1:p.Tyr507Ser
NM_001326314.1:c.1601A>C	NP_001313243.1:p.Tyr534Ser
NM_001326315.1:c.2039A>C	NP_001313244.1:p.Tyr680Ser
NM_001326316.1:c.2039A>C	NP_001313245.1:p.Tyr680Ser
NR_136936.1:n.2209A>C
XM_005268070.5:c.1748A>C	XP_005268127.1:p.Tyr583Ser
XM_005268073.4:c.1250A>C	XP_005268130.1:p.Tyr417Ser
XM_006720257.3:c.1175A>C	XP_006720320.1:p.Tyr392Ser
XM_011537161.3:c.1988A>C	XP_011535463.1:p.Tyr663Ser
XM_024449713.1:c.1172A>C	XP_024305481.1:p.Tyr391Ser
NM_024824.5:c.2144A>C MANE Select	NP_079100.2:p.Tyr715Ser
NM_001160103.2:c.2141A>C	NP_001153575.1:p.Tyr714Ser
NM_001160104.2:c.2126A>C	NP_001153576.1:p.Tyr709Ser
NM_001326295.2:c.1751A>C	NP_001313224.1:p.Tyr584Ser
NM_001326296.2:c.2066A>C	NP_001313225.1:p.Tyr689Ser
NM_001326297.2:c.2042A>C	NP_001313226.1:p.Tyr681Ser
NM_001326298.2:c.1676A>C	NP_001313227.1:p.Tyr559Ser
NM_001326299.2:c.2051A>C	NP_001313228.1:p.Tyr684Ser
NM_001326300.2:c.1679A>C	NP_001313229.1:p.Tyr560Ser
NM_001326301.2:c.1967A>C	NP_001313230.1:p.Tyr656Ser
NM_001326302.2:c.1676A>C	NP_001313231.1:p.Tyr559Ser
NM_001326303.2:c.1571A>C	NP_001313232.1:p.Tyr524Ser
NM_001326304.2:c.1283A>C	NP_001313233.1:p.Tyr428Ser
NM_001326305.2:c.1604A>C	NP_001313234.1:p.Tyr535Ser
NM_001326306.2:c.1517A>C	NP_001313235.1:p.Tyr506Ser
NM_001326307.2:c.2069A>C	NP_001313236.1:p.Tyr690Ser
NM_001326308.2:c.1286A>C	NP_001313237.1:p.Tyr429Ser
NM_001326309.2:c.1211A>C	NP_001313238.1:p.Tyr404Ser
NM_001326310.2:c.2129A>C	NP_001313239.1:p.Tyr710Ser
NM_001326311.2:c.1208A>C	NP_001313240.1:p.Tyr403Ser
NM_001326312.2:c.2054A>C	NP_001313241.1:p.Tyr685Ser
NM_001326313.2:c.1520A>C	NP_001313242.1:p.Tyr507Ser
NM_001326314.2:c.1601A>C	NP_001313243.1:p.Tyr534Ser
NM_001326315.2:c.2039A>C	NP_001313244.1:p.Tyr680Ser
NM_207660.4:c.1673A>C	NP_997543.1:p.Tyr558Ser
NM_207662.4:c.854A>C	NP_997545.2:p.Tyr285Ser
NR_136936.2:n.2081A>C
NM_001326316.2:c.2039A>C	NP_001313245.1:p.Tyr680Ser
NM_207661.3:c.1649A>C	NP_997544.1:p.Tyr550Ser