Canonical Allele Identifier: CA390566490

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077281C>T (hg19) ; chr14:g.88610937C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610937C>T , CM000676.2:g.88610937C>T	GRCh38
NC_000014.8:g.89077281C>T , CM000676.1:g.89077281C>T	GRCh37
NC_000014.7:g.88147034C>T	NCBI36
NG_050601.1:g.53029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2201C>T MANE Select	ENSP00000251038.5:p.Thr734Ile
ENST00000649731.1:c.*1409C>T	ENSP00000497757.1:n.*1409C>T
ENST00000251038.9:c.2201C>T	ENSP00000251038.5:p.Thr734Ile
ENST00000302216.12:c.1730C>T	ENSP00000307025.8:p.Thr577Ile
ENST00000318308.10:c.911C>T	ENSP00000327176.6:p.Thr304Ile
ENST00000336693.8:c.1706C>T	ENSP00000338002.4:p.Thr569Ile
ENST00000393514.9:c.2126C>T	ENSP00000377150.5:p.Thr709Ile
ENST00000406216.7:c.839C>T	ENSP00000384682.3:p.Thr280Ile
ENST00000554020.5:n.1044C>T
ENST00000555755.5:c.2183C>T	ENSP00000452475.1:p.Thr728Ile
ENST00000555792.1:c.446C>T	ENSP00000450823.1:p.Thr149Ile
ENST00000555851.6:n.360C>T
ENST00000555900.5:c.1307C>T	ENSP00000451530.1:p.Thr436Ile
ENST00000556000.5:c.1945C>T
ENST00000556945.5:c.1808C>T	ENSP00000450474.1:p.Thr603Ile
ENST00000557491.1:n.1486C>T
ENST00000557607.5:c.1253C>T	ENSP00000452370.1:p.Thr418Ile
NM_001160103.1:c.2198C>T	NP_001153575.1:p.Thr733Ile
NM_001160104.1:c.2183C>T	NP_001153576.1:p.Thr728Ile
NM_024824.4:c.2201C>T	NP_079100.2:p.Thr734Ile
NM_207660.3:c.1730C>T	NP_997543.1:p.Thr577Ile
NM_207661.2:c.1706C>T	NP_997544.1:p.Thr569Ile
NM_207662.3:c.911C>T	NP_997545.2:p.Thr304Ile
XM_005268067.3:c.2186C>T	XP_005268124.1:p.Thr729Ile
XM_005268068.3:c.2126C>T	XP_005268125.1:p.Thr709Ile
XM_005268069.3:c.1808C>T	XP_005268126.1:p.Thr603Ile
XM_005268070.3:c.1805C>T	XP_005268127.1:p.Thr602Ile
XM_005268071.3:c.1733C>T	XP_005268128.1:p.Thr578Ile
XM_005268073.3:c.1307C>T	XP_005268130.1:p.Thr436Ile
XM_006720257.2:c.1232C>T	XP_006720320.1:p.Thr411Ile
XM_011537160.1:c.2099C>T	XP_011535462.1:p.Thr700Ile
XM_011537161.1:c.2045C>T	XP_011535463.1:p.Thr682Ile
NM_001326295.1:c.1808C>T	NP_001313224.1:p.Thr603Ile
NM_001326296.1:c.2123C>T	NP_001313225.1:p.Thr708Ile
NM_001326297.1:c.2099C>T	NP_001313226.1:p.Thr700Ile
NM_001326298.1:c.1733C>T	NP_001313227.1:p.Thr578Ile
NM_001326299.1:c.2108C>T	NP_001313228.1:p.Thr703Ile
NM_001326300.1:c.1736C>T	NP_001313229.1:p.Thr579Ile
NM_001326301.1:c.2024C>T	NP_001313230.1:p.Thr675Ile
NM_001326302.1:c.1733C>T	NP_001313231.1:p.Thr578Ile
NM_001326303.1:c.1628C>T	NP_001313232.1:p.Thr543Ile
NM_001326304.1:c.1340C>T	NP_001313233.1:p.Thr447Ile
NM_001326305.1:c.1661C>T	NP_001313234.1:p.Thr554Ile
NM_001326306.1:c.1574C>T	NP_001313235.1:p.Thr525Ile
NM_001326307.1:c.2126C>T	NP_001313236.1:p.Thr709Ile
NM_001326308.1:c.1343C>T	NP_001313237.1:p.Thr448Ile
NM_001326309.1:c.1268C>T	NP_001313238.1:p.Thr423Ile
NM_001326310.1:c.2186C>T	NP_001313239.1:p.Thr729Ile
NM_001326311.1:c.1265C>T	NP_001313240.1:p.Thr422Ile
NM_001326312.1:c.2111C>T	NP_001313241.1:p.Thr704Ile
NM_001326313.1:c.1577C>T	NP_001313242.1:p.Thr526Ile
NM_001326314.1:c.1658C>T	NP_001313243.1:p.Thr553Ile
NM_001326315.1:c.2096C>T	NP_001313244.1:p.Thr699Ile
NM_001326316.1:c.2096C>T	NP_001313245.1:p.Thr699Ile
NR_136936.1:n.2266C>T
XM_005268070.5:c.1805C>T	XP_005268127.1:p.Thr602Ile
XM_005268073.4:c.1307C>T	XP_005268130.1:p.Thr436Ile
XM_006720257.3:c.1232C>T	XP_006720320.1:p.Thr411Ile
XM_011537161.3:c.2045C>T	XP_011535463.1:p.Thr682Ile
XM_024449713.1:c.1229C>T	XP_024305481.1:p.Thr410Ile
NM_024824.5:c.2201C>T MANE Select	NP_079100.2:p.Thr734Ile
NM_001160103.2:c.2198C>T	NP_001153575.1:p.Thr733Ile
NM_001160104.2:c.2183C>T	NP_001153576.1:p.Thr728Ile
NM_001326295.2:c.1808C>T	NP_001313224.1:p.Thr603Ile
NM_001326296.2:c.2123C>T	NP_001313225.1:p.Thr708Ile
NM_001326297.2:c.2099C>T	NP_001313226.1:p.Thr700Ile
NM_001326298.2:c.1733C>T	NP_001313227.1:p.Thr578Ile
NM_001326299.2:c.2108C>T	NP_001313228.1:p.Thr703Ile
NM_001326300.2:c.1736C>T	NP_001313229.1:p.Thr579Ile
NM_001326301.2:c.2024C>T	NP_001313230.1:p.Thr675Ile
NM_001326302.2:c.1733C>T	NP_001313231.1:p.Thr578Ile
NM_001326303.2:c.1628C>T	NP_001313232.1:p.Thr543Ile
NM_001326304.2:c.1340C>T	NP_001313233.1:p.Thr447Ile
NM_001326305.2:c.1661C>T	NP_001313234.1:p.Thr554Ile
NM_001326306.2:c.1574C>T	NP_001313235.1:p.Thr525Ile
NM_001326307.2:c.2126C>T	NP_001313236.1:p.Thr709Ile
NM_001326308.2:c.1343C>T	NP_001313237.1:p.Thr448Ile
NM_001326309.2:c.1268C>T	NP_001313238.1:p.Thr423Ile
NM_001326310.2:c.2186C>T	NP_001313239.1:p.Thr729Ile
NM_001326311.2:c.1265C>T	NP_001313240.1:p.Thr422Ile
NM_001326312.2:c.2111C>T	NP_001313241.1:p.Thr704Ile
NM_001326313.2:c.1577C>T	NP_001313242.1:p.Thr526Ile
NM_001326314.2:c.1658C>T	NP_001313243.1:p.Thr553Ile
NM_001326315.2:c.2096C>T	NP_001313244.1:p.Thr699Ile
NM_207660.4:c.1730C>T	NP_997543.1:p.Thr577Ile
NM_207662.4:c.911C>T	NP_997545.2:p.Thr304Ile
NR_136936.2:n.2138C>T
NM_001326316.2:c.2096C>T	NP_001313245.1:p.Thr699Ile
NM_207661.3:c.1706C>T	NP_997544.1:p.Thr569Ile