Canonical Allele Identifier: CA390566308

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077256G>T (hg19) ; chr14:g.88610912G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610912G>T , CM000676.2:g.88610912G>T	GRCh38
NC_000014.8:g.89077256G>T , CM000676.1:g.89077256G>T	GRCh37
NC_000014.7:g.88147009G>T	NCBI36
NG_050601.1:g.53004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2176G>T MANE Select	ENSP00000251038.5:p.Ala726Ser
ENST00000649731.1:c.*1384G>T	ENSP00000497757.1:n.*1384G>T
ENST00000251038.9:c.2176G>T	ENSP00000251038.5:p.Ala726Ser
ENST00000302216.12:c.1705G>T	ENSP00000307025.8:p.Ala569Ser
ENST00000318308.10:c.886G>T	ENSP00000327176.6:p.Ala296Ser
ENST00000336693.8:c.1681G>T	ENSP00000338002.4:p.Ala561Ser
ENST00000393514.9:c.2101G>T	ENSP00000377150.5:p.Ala701Ser
ENST00000406216.7:c.814G>T	ENSP00000384682.3:p.Ala272Ser
ENST00000554020.5:n.1019G>T
ENST00000555755.5:c.2158G>T	ENSP00000452475.1:p.Ala720Ser
ENST00000555792.1:c.421G>T	ENSP00000450823.1:p.Ala141Ser
ENST00000555851.6:n.335G>T
ENST00000555900.5:c.1282G>T	ENSP00000451530.1:p.Ala428Ser
ENST00000556000.5:c.1920G>T
ENST00000556945.5:c.1783G>T	ENSP00000450474.1:p.Ala595Ser
ENST00000557491.1:n.1461G>T
ENST00000557607.5:c.1228G>T	ENSP00000452370.1:p.Ala410Ser
NM_001160103.1:c.2173G>T	NP_001153575.1:p.Ala725Ser
NM_001160104.1:c.2158G>T	NP_001153576.1:p.Ala720Ser
NM_024824.4:c.2176G>T	NP_079100.2:p.Ala726Ser
NM_207660.3:c.1705G>T	NP_997543.1:p.Ala569Ser
NM_207661.2:c.1681G>T	NP_997544.1:p.Ala561Ser
NM_207662.3:c.886G>T	NP_997545.2:p.Ala296Ser
XM_005268067.3:c.2161G>T	XP_005268124.1:p.Ala721Ser
XM_005268068.3:c.2101G>T	XP_005268125.1:p.Ala701Ser
XM_005268069.3:c.1783G>T	XP_005268126.1:p.Ala595Ser
XM_005268070.3:c.1780G>T	XP_005268127.1:p.Ala594Ser
XM_005268071.3:c.1708G>T	XP_005268128.1:p.Ala570Ser
XM_005268073.3:c.1282G>T	XP_005268130.1:p.Ala428Ser
XM_006720257.2:c.1207G>T	XP_006720320.1:p.Ala403Ser
XM_011537160.1:c.2074G>T	XP_011535462.1:p.Ala692Ser
XM_011537161.1:c.2020G>T	XP_011535463.1:p.Ala674Ser
NM_001326295.1:c.1783G>T	NP_001313224.1:p.Ala595Ser
NM_001326296.1:c.2098G>T	NP_001313225.1:p.Ala700Ser
NM_001326297.1:c.2074G>T	NP_001313226.1:p.Ala692Ser
NM_001326298.1:c.1708G>T	NP_001313227.1:p.Ala570Ser
NM_001326299.1:c.2083G>T	NP_001313228.1:p.Ala695Ser
NM_001326300.1:c.1711G>T	NP_001313229.1:p.Ala571Ser
NM_001326301.1:c.1999G>T	NP_001313230.1:p.Ala667Ser
NM_001326302.1:c.1708G>T	NP_001313231.1:p.Ala570Ser
NM_001326303.1:c.1603G>T	NP_001313232.1:p.Ala535Ser
NM_001326304.1:c.1315G>T	NP_001313233.1:p.Ala439Ser
NM_001326305.1:c.1636G>T	NP_001313234.1:p.Ala546Ser
NM_001326306.1:c.1549G>T	NP_001313235.1:p.Ala517Ser
NM_001326307.1:c.2101G>T	NP_001313236.1:p.Ala701Ser
NM_001326308.1:c.1318G>T	NP_001313237.1:p.Ala440Ser
NM_001326309.1:c.1243G>T	NP_001313238.1:p.Ala415Ser
NM_001326310.1:c.2161G>T	NP_001313239.1:p.Ala721Ser
NM_001326311.1:c.1240G>T	NP_001313240.1:p.Ala414Ser
NM_001326312.1:c.2086G>T	NP_001313241.1:p.Ala696Ser
NM_001326313.1:c.1552G>T	NP_001313242.1:p.Ala518Ser
NM_001326314.1:c.1633G>T	NP_001313243.1:p.Ala545Ser
NM_001326315.1:c.2071G>T	NP_001313244.1:p.Ala691Ser
NM_001326316.1:c.2071G>T	NP_001313245.1:p.Ala691Ser
NR_136936.1:n.2241G>T
XM_005268070.5:c.1780G>T	XP_005268127.1:p.Ala594Ser
XM_005268073.4:c.1282G>T	XP_005268130.1:p.Ala428Ser
XM_006720257.3:c.1207G>T	XP_006720320.1:p.Ala403Ser
XM_011537161.3:c.2020G>T	XP_011535463.1:p.Ala674Ser
XM_024449713.1:c.1204G>T	XP_024305481.1:p.Ala402Ser
NM_024824.5:c.2176G>T MANE Select	NP_079100.2:p.Ala726Ser
NM_001160103.2:c.2173G>T	NP_001153575.1:p.Ala725Ser
NM_001160104.2:c.2158G>T	NP_001153576.1:p.Ala720Ser
NM_001326295.2:c.1783G>T	NP_001313224.1:p.Ala595Ser
NM_001326296.2:c.2098G>T	NP_001313225.1:p.Ala700Ser
NM_001326297.2:c.2074G>T	NP_001313226.1:p.Ala692Ser
NM_001326298.2:c.1708G>T	NP_001313227.1:p.Ala570Ser
NM_001326299.2:c.2083G>T	NP_001313228.1:p.Ala695Ser
NM_001326300.2:c.1711G>T	NP_001313229.1:p.Ala571Ser
NM_001326301.2:c.1999G>T	NP_001313230.1:p.Ala667Ser
NM_001326302.2:c.1708G>T	NP_001313231.1:p.Ala570Ser
NM_001326303.2:c.1603G>T	NP_001313232.1:p.Ala535Ser
NM_001326304.2:c.1315G>T	NP_001313233.1:p.Ala439Ser
NM_001326305.2:c.1636G>T	NP_001313234.1:p.Ala546Ser
NM_001326306.2:c.1549G>T	NP_001313235.1:p.Ala517Ser
NM_001326307.2:c.2101G>T	NP_001313236.1:p.Ala701Ser
NM_001326308.2:c.1318G>T	NP_001313237.1:p.Ala440Ser
NM_001326309.2:c.1243G>T	NP_001313238.1:p.Ala415Ser
NM_001326310.2:c.2161G>T	NP_001313239.1:p.Ala721Ser
NM_001326311.2:c.1240G>T	NP_001313240.1:p.Ala414Ser
NM_001326312.2:c.2086G>T	NP_001313241.1:p.Ala696Ser
NM_001326313.2:c.1552G>T	NP_001313242.1:p.Ala518Ser
NM_001326314.2:c.1633G>T	NP_001313243.1:p.Ala545Ser
NM_001326315.2:c.2071G>T	NP_001313244.1:p.Ala691Ser
NM_207660.4:c.1705G>T	NP_997543.1:p.Ala569Ser
NM_207662.4:c.886G>T	NP_997545.2:p.Ala296Ser
NR_136936.2:n.2113G>T
NM_001326316.2:c.2071G>T	NP_001313245.1:p.Ala691Ser
NM_207661.3:c.1681G>T	NP_997544.1:p.Ala561Ser