Canonical Allele Identifier: CA390566484

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077280A>T (hg19) ; chr14:g.88610936A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610936A>T , CM000676.2:g.88610936A>T	GRCh38
NC_000014.8:g.89077280A>T , CM000676.1:g.89077280A>T	GRCh37
NC_000014.7:g.88147033A>T	NCBI36
NG_050601.1:g.53028A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2200A>T MANE Select	ENSP00000251038.5:p.Thr734Ser
ENST00000649731.1:c.*1408A>T	ENSP00000497757.1:n.*1408A>T
ENST00000251038.9:c.2200A>T	ENSP00000251038.5:p.Thr734Ser
ENST00000302216.12:c.1729A>T	ENSP00000307025.8:p.Thr577Ser
ENST00000318308.10:c.910A>T	ENSP00000327176.6:p.Thr304Ser
ENST00000336693.8:c.1705A>T	ENSP00000338002.4:p.Thr569Ser
ENST00000393514.9:c.2125A>T	ENSP00000377150.5:p.Thr709Ser
ENST00000406216.7:c.838A>T	ENSP00000384682.3:p.Thr280Ser
ENST00000554020.5:n.1043A>T
ENST00000555755.5:c.2182A>T	ENSP00000452475.1:p.Thr728Ser
ENST00000555792.1:c.445A>T	ENSP00000450823.1:p.Thr149Ser
ENST00000555851.6:n.359A>T
ENST00000555900.5:c.1306A>T	ENSP00000451530.1:p.Thr436Ser
ENST00000556000.5:c.1944A>T
ENST00000556945.5:c.1807A>T	ENSP00000450474.1:p.Thr603Ser
ENST00000557491.1:n.1485A>T
ENST00000557607.5:c.1252A>T	ENSP00000452370.1:p.Thr418Ser
NM_001160103.1:c.2197A>T	NP_001153575.1:p.Thr733Ser
NM_001160104.1:c.2182A>T	NP_001153576.1:p.Thr728Ser
NM_024824.4:c.2200A>T	NP_079100.2:p.Thr734Ser
NM_207660.3:c.1729A>T	NP_997543.1:p.Thr577Ser
NM_207661.2:c.1705A>T	NP_997544.1:p.Thr569Ser
NM_207662.3:c.910A>T	NP_997545.2:p.Thr304Ser
XM_005268067.3:c.2185A>T	XP_005268124.1:p.Thr729Ser
XM_005268068.3:c.2125A>T	XP_005268125.1:p.Thr709Ser
XM_005268069.3:c.1807A>T	XP_005268126.1:p.Thr603Ser
XM_005268070.3:c.1804A>T	XP_005268127.1:p.Thr602Ser
XM_005268071.3:c.1732A>T	XP_005268128.1:p.Thr578Ser
XM_005268073.3:c.1306A>T	XP_005268130.1:p.Thr436Ser
XM_006720257.2:c.1231A>T	XP_006720320.1:p.Thr411Ser
XM_011537160.1:c.2098A>T	XP_011535462.1:p.Thr700Ser
XM_011537161.1:c.2044A>T	XP_011535463.1:p.Thr682Ser
NM_001326295.1:c.1807A>T	NP_001313224.1:p.Thr603Ser
NM_001326296.1:c.2122A>T	NP_001313225.1:p.Thr708Ser
NM_001326297.1:c.2098A>T	NP_001313226.1:p.Thr700Ser
NM_001326298.1:c.1732A>T	NP_001313227.1:p.Thr578Ser
NM_001326299.1:c.2107A>T	NP_001313228.1:p.Thr703Ser
NM_001326300.1:c.1735A>T	NP_001313229.1:p.Thr579Ser
NM_001326301.1:c.2023A>T	NP_001313230.1:p.Thr675Ser
NM_001326302.1:c.1732A>T	NP_001313231.1:p.Thr578Ser
NM_001326303.1:c.1627A>T	NP_001313232.1:p.Thr543Ser
NM_001326304.1:c.1339A>T	NP_001313233.1:p.Thr447Ser
NM_001326305.1:c.1660A>T	NP_001313234.1:p.Thr554Ser
NM_001326306.1:c.1573A>T	NP_001313235.1:p.Thr525Ser
NM_001326307.1:c.2125A>T	NP_001313236.1:p.Thr709Ser
NM_001326308.1:c.1342A>T	NP_001313237.1:p.Thr448Ser
NM_001326309.1:c.1267A>T	NP_001313238.1:p.Thr423Ser
NM_001326310.1:c.2185A>T	NP_001313239.1:p.Thr729Ser
NM_001326311.1:c.1264A>T	NP_001313240.1:p.Thr422Ser
NM_001326312.1:c.2110A>T	NP_001313241.1:p.Thr704Ser
NM_001326313.1:c.1576A>T	NP_001313242.1:p.Thr526Ser
NM_001326314.1:c.1657A>T	NP_001313243.1:p.Thr553Ser
NM_001326315.1:c.2095A>T	NP_001313244.1:p.Thr699Ser
NM_001326316.1:c.2095A>T	NP_001313245.1:p.Thr699Ser
NR_136936.1:n.2265A>T
XM_005268070.5:c.1804A>T	XP_005268127.1:p.Thr602Ser
XM_005268073.4:c.1306A>T	XP_005268130.1:p.Thr436Ser
XM_006720257.3:c.1231A>T	XP_006720320.1:p.Thr411Ser
XM_011537161.3:c.2044A>T	XP_011535463.1:p.Thr682Ser
XM_024449713.1:c.1228A>T	XP_024305481.1:p.Thr410Ser
NM_024824.5:c.2200A>T MANE Select	NP_079100.2:p.Thr734Ser
NM_001160103.2:c.2197A>T	NP_001153575.1:p.Thr733Ser
NM_001160104.2:c.2182A>T	NP_001153576.1:p.Thr728Ser
NM_001326295.2:c.1807A>T	NP_001313224.1:p.Thr603Ser
NM_001326296.2:c.2122A>T	NP_001313225.1:p.Thr708Ser
NM_001326297.2:c.2098A>T	NP_001313226.1:p.Thr700Ser
NM_001326298.2:c.1732A>T	NP_001313227.1:p.Thr578Ser
NM_001326299.2:c.2107A>T	NP_001313228.1:p.Thr703Ser
NM_001326300.2:c.1735A>T	NP_001313229.1:p.Thr579Ser
NM_001326301.2:c.2023A>T	NP_001313230.1:p.Thr675Ser
NM_001326302.2:c.1732A>T	NP_001313231.1:p.Thr578Ser
NM_001326303.2:c.1627A>T	NP_001313232.1:p.Thr543Ser
NM_001326304.2:c.1339A>T	NP_001313233.1:p.Thr447Ser
NM_001326305.2:c.1660A>T	NP_001313234.1:p.Thr554Ser
NM_001326306.2:c.1573A>T	NP_001313235.1:p.Thr525Ser
NM_001326307.2:c.2125A>T	NP_001313236.1:p.Thr709Ser
NM_001326308.2:c.1342A>T	NP_001313237.1:p.Thr448Ser
NM_001326309.2:c.1267A>T	NP_001313238.1:p.Thr423Ser
NM_001326310.2:c.2185A>T	NP_001313239.1:p.Thr729Ser
NM_001326311.2:c.1264A>T	NP_001313240.1:p.Thr422Ser
NM_001326312.2:c.2110A>T	NP_001313241.1:p.Thr704Ser
NM_001326313.2:c.1576A>T	NP_001313242.1:p.Thr526Ser
NM_001326314.2:c.1657A>T	NP_001313243.1:p.Thr553Ser
NM_001326315.2:c.2095A>T	NP_001313244.1:p.Thr699Ser
NM_207660.4:c.1729A>T	NP_997543.1:p.Thr577Ser
NM_207662.4:c.910A>T	NP_997545.2:p.Thr304Ser
NR_136936.2:n.2137A>T
NM_001326316.2:c.2095A>T	NP_001313245.1:p.Thr699Ser
NM_207661.3:c.1705A>T	NP_997544.1:p.Thr569Ser