Canonical Allele Identifier: CA390566363

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077265T>A (hg19) ; chr14:g.88610921T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610921T>A , CM000676.2:g.88610921T>A	GRCh38
NC_000014.8:g.89077265T>A , CM000676.1:g.89077265T>A	GRCh37
NC_000014.7:g.88147018T>A	NCBI36
NG_050601.1:g.53013T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2185T>A MANE Select	ENSP00000251038.5:p.Trp729Arg
ENST00000649731.1:c.*1393T>A	ENSP00000497757.1:n.*1393T>A
ENST00000251038.9:c.2185T>A	ENSP00000251038.5:p.Trp729Arg
ENST00000302216.12:c.1714T>A	ENSP00000307025.8:p.Trp572Arg
ENST00000318308.10:c.895T>A	ENSP00000327176.6:p.Trp299Arg
ENST00000336693.8:c.1690T>A	ENSP00000338002.4:p.Trp564Arg
ENST00000393514.9:c.2110T>A	ENSP00000377150.5:p.Trp704Arg
ENST00000406216.7:c.823T>A	ENSP00000384682.3:p.Trp275Arg
ENST00000554020.5:n.1028T>A
ENST00000555755.5:c.2167T>A	ENSP00000452475.1:p.Trp723Arg
ENST00000555792.1:c.430T>A	ENSP00000450823.1:p.Trp144Arg
ENST00000555851.6:n.344T>A
ENST00000555900.5:c.1291T>A	ENSP00000451530.1:p.Trp431Arg
ENST00000556000.5:c.1929T>A
ENST00000556945.5:c.1792T>A	ENSP00000450474.1:p.Trp598Arg
ENST00000557491.1:n.1470T>A
ENST00000557607.5:c.1237T>A	ENSP00000452370.1:p.Trp413Arg
NM_001160103.1:c.2182T>A	NP_001153575.1:p.Trp728Arg
NM_001160104.1:c.2167T>A	NP_001153576.1:p.Trp723Arg
NM_024824.4:c.2185T>A	NP_079100.2:p.Trp729Arg
NM_207660.3:c.1714T>A	NP_997543.1:p.Trp572Arg
NM_207661.2:c.1690T>A	NP_997544.1:p.Trp564Arg
NM_207662.3:c.895T>A	NP_997545.2:p.Trp299Arg
XM_005268067.3:c.2170T>A	XP_005268124.1:p.Trp724Arg
XM_005268068.3:c.2110T>A	XP_005268125.1:p.Trp704Arg
XM_005268069.3:c.1792T>A	XP_005268126.1:p.Trp598Arg
XM_005268070.3:c.1789T>A	XP_005268127.1:p.Trp597Arg
XM_005268071.3:c.1717T>A	XP_005268128.1:p.Trp573Arg
XM_005268073.3:c.1291T>A	XP_005268130.1:p.Trp431Arg
XM_006720257.2:c.1216T>A	XP_006720320.1:p.Trp406Arg
XM_011537160.1:c.2083T>A	XP_011535462.1:p.Trp695Arg
XM_011537161.1:c.2029T>A	XP_011535463.1:p.Trp677Arg
NM_001326295.1:c.1792T>A	NP_001313224.1:p.Trp598Arg
NM_001326296.1:c.2107T>A	NP_001313225.1:p.Trp703Arg
NM_001326297.1:c.2083T>A	NP_001313226.1:p.Trp695Arg
NM_001326298.1:c.1717T>A	NP_001313227.1:p.Trp573Arg
NM_001326299.1:c.2092T>A	NP_001313228.1:p.Trp698Arg
NM_001326300.1:c.1720T>A	NP_001313229.1:p.Trp574Arg
NM_001326301.1:c.2008T>A	NP_001313230.1:p.Trp670Arg
NM_001326302.1:c.1717T>A	NP_001313231.1:p.Trp573Arg
NM_001326303.1:c.1612T>A	NP_001313232.1:p.Trp538Arg
NM_001326304.1:c.1324T>A	NP_001313233.1:p.Trp442Arg
NM_001326305.1:c.1645T>A	NP_001313234.1:p.Trp549Arg
NM_001326306.1:c.1558T>A	NP_001313235.1:p.Trp520Arg
NM_001326307.1:c.2110T>A	NP_001313236.1:p.Trp704Arg
NM_001326308.1:c.1327T>A	NP_001313237.1:p.Trp443Arg
NM_001326309.1:c.1252T>A	NP_001313238.1:p.Trp418Arg
NM_001326310.1:c.2170T>A	NP_001313239.1:p.Trp724Arg
NM_001326311.1:c.1249T>A	NP_001313240.1:p.Trp417Arg
NM_001326312.1:c.2095T>A	NP_001313241.1:p.Trp699Arg
NM_001326313.1:c.1561T>A	NP_001313242.1:p.Trp521Arg
NM_001326314.1:c.1642T>A	NP_001313243.1:p.Trp548Arg
NM_001326315.1:c.2080T>A	NP_001313244.1:p.Trp694Arg
NM_001326316.1:c.2080T>A	NP_001313245.1:p.Trp694Arg
NR_136936.1:n.2250T>A
XM_005268070.5:c.1789T>A	XP_005268127.1:p.Trp597Arg
XM_005268073.4:c.1291T>A	XP_005268130.1:p.Trp431Arg
XM_006720257.3:c.1216T>A	XP_006720320.1:p.Trp406Arg
XM_011537161.3:c.2029T>A	XP_011535463.1:p.Trp677Arg
XM_024449713.1:c.1213T>A	XP_024305481.1:p.Trp405Arg
NM_024824.5:c.2185T>A MANE Select	NP_079100.2:p.Trp729Arg
NM_001160103.2:c.2182T>A	NP_001153575.1:p.Trp728Arg
NM_001160104.2:c.2167T>A	NP_001153576.1:p.Trp723Arg
NM_001326295.2:c.1792T>A	NP_001313224.1:p.Trp598Arg
NM_001326296.2:c.2107T>A	NP_001313225.1:p.Trp703Arg
NM_001326297.2:c.2083T>A	NP_001313226.1:p.Trp695Arg
NM_001326298.2:c.1717T>A	NP_001313227.1:p.Trp573Arg
NM_001326299.2:c.2092T>A	NP_001313228.1:p.Trp698Arg
NM_001326300.2:c.1720T>A	NP_001313229.1:p.Trp574Arg
NM_001326301.2:c.2008T>A	NP_001313230.1:p.Trp670Arg
NM_001326302.2:c.1717T>A	NP_001313231.1:p.Trp573Arg
NM_001326303.2:c.1612T>A	NP_001313232.1:p.Trp538Arg
NM_001326304.2:c.1324T>A	NP_001313233.1:p.Trp442Arg
NM_001326305.2:c.1645T>A	NP_001313234.1:p.Trp549Arg
NM_001326306.2:c.1558T>A	NP_001313235.1:p.Trp520Arg
NM_001326307.2:c.2110T>A	NP_001313236.1:p.Trp704Arg
NM_001326308.2:c.1327T>A	NP_001313237.1:p.Trp443Arg
NM_001326309.2:c.1252T>A	NP_001313238.1:p.Trp418Arg
NM_001326310.2:c.2170T>A	NP_001313239.1:p.Trp724Arg
NM_001326311.2:c.1249T>A	NP_001313240.1:p.Trp417Arg
NM_001326312.2:c.2095T>A	NP_001313241.1:p.Trp699Arg
NM_001326313.2:c.1561T>A	NP_001313242.1:p.Trp521Arg
NM_001326314.2:c.1642T>A	NP_001313243.1:p.Trp548Arg
NM_001326315.2:c.2080T>A	NP_001313244.1:p.Trp694Arg
NM_207660.4:c.1714T>A	NP_997543.1:p.Trp572Arg
NM_207662.4:c.895T>A	NP_997545.2:p.Trp299Arg
NR_136936.2:n.2122T>A
NM_001326316.2:c.2080T>A	NP_001313245.1:p.Trp694Arg
NM_207661.3:c.1690T>A	NP_997544.1:p.Trp564Arg