Canonical Allele Identifier: CA390566494

Gene: ZC3H14

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2201C>G MANE Select	ENSP00000251038.5:p.Thr734Ser
ENST00000649731.1:c.*1409C>G	ENSP00000497757.1:n.*1409C>G
ENST00000251038.9:c.2201C>G	ENSP00000251038.5:p.Thr734Ser
ENST00000302216.12:c.1730C>G	ENSP00000307025.8:p.Thr577Ser
ENST00000318308.10:c.911C>G	ENSP00000327176.6:p.Thr304Ser
ENST00000336693.8:c.1706C>G	ENSP00000338002.4:p.Thr569Ser
ENST00000393514.9:c.2126C>G	ENSP00000377150.5:p.Thr709Ser
ENST00000406216.7:c.839C>G	ENSP00000384682.3:p.Thr280Ser
ENST00000554020.5:n.1044C>G
ENST00000555755.5:c.2183C>G	ENSP00000452475.1:p.Thr728Ser
ENST00000555792.1:c.446C>G	ENSP00000450823.1:p.Thr149Ser
ENST00000555851.6:n.360C>G
ENST00000555900.5:c.1307C>G	ENSP00000451530.1:p.Thr436Ser
ENST00000556000.5:c.1945C>G
ENST00000556945.5:c.1808C>G	ENSP00000450474.1:p.Thr603Ser
ENST00000557491.1:n.1486C>G
ENST00000557607.5:c.1253C>G	ENSP00000452370.1:p.Thr418Ser
NM_001160103.1:c.2198C>G	NP_001153575.1:p.Thr733Ser
NM_001160104.1:c.2183C>G	NP_001153576.1:p.Thr728Ser
NM_024824.4:c.2201C>G	NP_079100.2:p.Thr734Ser
NM_207660.3:c.1730C>G	NP_997543.1:p.Thr577Ser
NM_207661.2:c.1706C>G	NP_997544.1:p.Thr569Ser
NM_207662.3:c.911C>G	NP_997545.2:p.Thr304Ser
XM_005268067.3:c.2186C>G	XP_005268124.1:p.Thr729Ser
XM_005268068.3:c.2126C>G	XP_005268125.1:p.Thr709Ser
XM_005268069.3:c.1808C>G	XP_005268126.1:p.Thr603Ser
XM_005268070.3:c.1805C>G	XP_005268127.1:p.Thr602Ser
XM_005268071.3:c.1733C>G	XP_005268128.1:p.Thr578Ser
XM_005268073.3:c.1307C>G	XP_005268130.1:p.Thr436Ser
XM_006720257.2:c.1232C>G	XP_006720320.1:p.Thr411Ser
XM_011537160.1:c.2099C>G	XP_011535462.1:p.Thr700Ser
XM_011537161.1:c.2045C>G	XP_011535463.1:p.Thr682Ser
NM_001326295.1:c.1808C>G	NP_001313224.1:p.Thr603Ser
NM_001326296.1:c.2123C>G	NP_001313225.1:p.Thr708Ser
NM_001326297.1:c.2099C>G	NP_001313226.1:p.Thr700Ser
NM_001326298.1:c.1733C>G	NP_001313227.1:p.Thr578Ser
NM_001326299.1:c.2108C>G	NP_001313228.1:p.Thr703Ser
NM_001326300.1:c.1736C>G	NP_001313229.1:p.Thr579Ser
NM_001326301.1:c.2024C>G	NP_001313230.1:p.Thr675Ser
NM_001326302.1:c.1733C>G	NP_001313231.1:p.Thr578Ser
NM_001326303.1:c.1628C>G	NP_001313232.1:p.Thr543Ser
NM_001326304.1:c.1340C>G	NP_001313233.1:p.Thr447Ser
NM_001326305.1:c.1661C>G	NP_001313234.1:p.Thr554Ser
NM_001326306.1:c.1574C>G	NP_001313235.1:p.Thr525Ser
NM_001326307.1:c.2126C>G	NP_001313236.1:p.Thr709Ser
NM_001326308.1:c.1343C>G	NP_001313237.1:p.Thr448Ser
NM_001326309.1:c.1268C>G	NP_001313238.1:p.Thr423Ser
NM_001326310.1:c.2186C>G	NP_001313239.1:p.Thr729Ser
NM_001326311.1:c.1265C>G	NP_001313240.1:p.Thr422Ser
NM_001326312.1:c.2111C>G	NP_001313241.1:p.Thr704Ser
NM_001326313.1:c.1577C>G	NP_001313242.1:p.Thr526Ser
NM_001326314.1:c.1658C>G	NP_001313243.1:p.Thr553Ser
NM_001326315.1:c.2096C>G	NP_001313244.1:p.Thr699Ser
NM_001326316.1:c.2096C>G	NP_001313245.1:p.Thr699Ser
NR_136936.1:n.2266C>G
XM_005268070.5:c.1805C>G	XP_005268127.1:p.Thr602Ser
XM_005268073.4:c.1307C>G	XP_005268130.1:p.Thr436Ser
XM_006720257.3:c.1232C>G	XP_006720320.1:p.Thr411Ser
XM_011537161.3:c.2045C>G	XP_011535463.1:p.Thr682Ser
XM_024449713.1:c.1229C>G	XP_024305481.1:p.Thr410Ser
NM_024824.5:c.2201C>G MANE Select	NP_079100.2:p.Thr734Ser
NM_001160103.2:c.2198C>G	NP_001153575.1:p.Thr733Ser
NM_001160104.2:c.2183C>G	NP_001153576.1:p.Thr728Ser
NM_001326295.2:c.1808C>G	NP_001313224.1:p.Thr603Ser
NM_001326296.2:c.2123C>G	NP_001313225.1:p.Thr708Ser
NM_001326297.2:c.2099C>G	NP_001313226.1:p.Thr700Ser
NM_001326298.2:c.1733C>G	NP_001313227.1:p.Thr578Ser
NM_001326299.2:c.2108C>G	NP_001313228.1:p.Thr703Ser
NM_001326300.2:c.1736C>G	NP_001313229.1:p.Thr579Ser
NM_001326301.2:c.2024C>G	NP_001313230.1:p.Thr675Ser
NM_001326302.2:c.1733C>G	NP_001313231.1:p.Thr578Ser
NM_001326303.2:c.1628C>G	NP_001313232.1:p.Thr543Ser
NM_001326304.2:c.1340C>G	NP_001313233.1:p.Thr447Ser
NM_001326305.2:c.1661C>G	NP_001313234.1:p.Thr554Ser
NM_001326306.2:c.1574C>G	NP_001313235.1:p.Thr525Ser
NM_001326307.2:c.2126C>G	NP_001313236.1:p.Thr709Ser
NM_001326308.2:c.1343C>G	NP_001313237.1:p.Thr448Ser
NM_001326309.2:c.1268C>G	NP_001313238.1:p.Thr423Ser
NM_001326310.2:c.2186C>G	NP_001313239.1:p.Thr729Ser
NM_001326311.2:c.1265C>G	NP_001313240.1:p.Thr422Ser
NM_001326312.2:c.2111C>G	NP_001313241.1:p.Thr704Ser
NM_001326313.2:c.1577C>G	NP_001313242.1:p.Thr526Ser
NM_001326314.2:c.1658C>G	NP_001313243.1:p.Thr553Ser
NM_001326315.2:c.2096C>G	NP_001313244.1:p.Thr699Ser
NM_207660.4:c.1730C>G	NP_997543.1:p.Thr577Ser
NM_207662.4:c.911C>G	NP_997545.2:p.Thr304Ser
NR_136936.2:n.2138C>G
NM_001326316.2:c.2096C>G	NP_001313245.1:p.Thr699Ser
NM_207661.3:c.1706C>G	NP_997544.1:p.Thr569Ser