Canonical Allele Identifier: CA390566045

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077226C>G (hg19) ; chr14:g.88610882C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610882C>G , CM000676.2:g.88610882C>G	GRCh38
NC_000014.8:g.89077226C>G , CM000676.1:g.89077226C>G	GRCh37
NC_000014.7:g.88146979C>G	NCBI36
NG_050601.1:g.52974C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2146C>G MANE Select	ENSP00000251038.5:p.His716Asp
ENST00000649731.1:c.*1354C>G	ENSP00000497757.1:n.*1354C>G
ENST00000251038.9:c.2146C>G	ENSP00000251038.5:p.His716Asp
ENST00000302216.12:c.1675C>G	ENSP00000307025.8:p.His559Asp
ENST00000318308.10:c.856C>G	ENSP00000327176.6:p.His286Asp
ENST00000336693.8:c.1651C>G	ENSP00000338002.4:p.His551Asp
ENST00000393514.9:c.2071C>G	ENSP00000377150.5:p.His691Asp
ENST00000406216.7:c.784C>G	ENSP00000384682.3:p.His262Asp
ENST00000554020.5:n.989C>G
ENST00000555755.5:c.2128C>G	ENSP00000452475.1:p.His710Asp
ENST00000555792.1:c.391C>G	ENSP00000450823.1:p.His131Asp
ENST00000555851.6:n.305C>G
ENST00000555900.5:c.1252C>G	ENSP00000451530.1:p.His418Asp
ENST00000556000.5:c.1890C>G
ENST00000556945.5:c.1753C>G	ENSP00000450474.1:p.His585Asp
ENST00000557491.1:n.1431C>G
ENST00000557607.5:c.1198C>G	ENSP00000452370.1:p.His400Asp
NM_001160103.1:c.2143C>G	NP_001153575.1:p.His715Asp
NM_001160104.1:c.2128C>G	NP_001153576.1:p.His710Asp
NM_024824.4:c.2146C>G	NP_079100.2:p.His716Asp
NM_207660.3:c.1675C>G	NP_997543.1:p.His559Asp
NM_207661.2:c.1651C>G	NP_997544.1:p.His551Asp
NM_207662.3:c.856C>G	NP_997545.2:p.His286Asp
XM_005268067.3:c.2131C>G	XP_005268124.1:p.His711Asp
XM_005268068.3:c.2071C>G	XP_005268125.1:p.His691Asp
XM_005268069.3:c.1753C>G	XP_005268126.1:p.His585Asp
XM_005268070.3:c.1750C>G	XP_005268127.1:p.His584Asp
XM_005268071.3:c.1678C>G	XP_005268128.1:p.His560Asp
XM_005268073.3:c.1252C>G	XP_005268130.1:p.His418Asp
XM_006720257.2:c.1177C>G	XP_006720320.1:p.His393Asp
XM_011537160.1:c.2044C>G	XP_011535462.1:p.His682Asp
XM_011537161.1:c.1990C>G	XP_011535463.1:p.His664Asp
NM_001326295.1:c.1753C>G	NP_001313224.1:p.His585Asp
NM_001326296.1:c.2068C>G	NP_001313225.1:p.His690Asp
NM_001326297.1:c.2044C>G	NP_001313226.1:p.His682Asp
NM_001326298.1:c.1678C>G	NP_001313227.1:p.His560Asp
NM_001326299.1:c.2053C>G	NP_001313228.1:p.His685Asp
NM_001326300.1:c.1681C>G	NP_001313229.1:p.His561Asp
NM_001326301.1:c.1969C>G	NP_001313230.1:p.His657Asp
NM_001326302.1:c.1678C>G	NP_001313231.1:p.His560Asp
NM_001326303.1:c.1573C>G	NP_001313232.1:p.His525Asp
NM_001326304.1:c.1285C>G	NP_001313233.1:p.His429Asp
NM_001326305.1:c.1606C>G	NP_001313234.1:p.His536Asp
NM_001326306.1:c.1519C>G	NP_001313235.1:p.His507Asp
NM_001326307.1:c.2071C>G	NP_001313236.1:p.His691Asp
NM_001326308.1:c.1288C>G	NP_001313237.1:p.His430Asp
NM_001326309.1:c.1213C>G	NP_001313238.1:p.His405Asp
NM_001326310.1:c.2131C>G	NP_001313239.1:p.His711Asp
NM_001326311.1:c.1210C>G	NP_001313240.1:p.His404Asp
NM_001326312.1:c.2056C>G	NP_001313241.1:p.His686Asp
NM_001326313.1:c.1522C>G	NP_001313242.1:p.His508Asp
NM_001326314.1:c.1603C>G	NP_001313243.1:p.His535Asp
NM_001326315.1:c.2041C>G	NP_001313244.1:p.His681Asp
NM_001326316.1:c.2041C>G	NP_001313245.1:p.His681Asp
NR_136936.1:n.2211C>G
XM_005268070.5:c.1750C>G	XP_005268127.1:p.His584Asp
XM_005268073.4:c.1252C>G	XP_005268130.1:p.His418Asp
XM_006720257.3:c.1177C>G	XP_006720320.1:p.His393Asp
XM_011537161.3:c.1990C>G	XP_011535463.1:p.His664Asp
XM_024449713.1:c.1174C>G	XP_024305481.1:p.His392Asp
NM_024824.5:c.2146C>G MANE Select	NP_079100.2:p.His716Asp
NM_001160103.2:c.2143C>G	NP_001153575.1:p.His715Asp
NM_001160104.2:c.2128C>G	NP_001153576.1:p.His710Asp
NM_001326295.2:c.1753C>G	NP_001313224.1:p.His585Asp
NM_001326296.2:c.2068C>G	NP_001313225.1:p.His690Asp
NM_001326297.2:c.2044C>G	NP_001313226.1:p.His682Asp
NM_001326298.2:c.1678C>G	NP_001313227.1:p.His560Asp
NM_001326299.2:c.2053C>G	NP_001313228.1:p.His685Asp
NM_001326300.2:c.1681C>G	NP_001313229.1:p.His561Asp
NM_001326301.2:c.1969C>G	NP_001313230.1:p.His657Asp
NM_001326302.2:c.1678C>G	NP_001313231.1:p.His560Asp
NM_001326303.2:c.1573C>G	NP_001313232.1:p.His525Asp
NM_001326304.2:c.1285C>G	NP_001313233.1:p.His429Asp
NM_001326305.2:c.1606C>G	NP_001313234.1:p.His536Asp
NM_001326306.2:c.1519C>G	NP_001313235.1:p.His507Asp
NM_001326307.2:c.2071C>G	NP_001313236.1:p.His691Asp
NM_001326308.2:c.1288C>G	NP_001313237.1:p.His430Asp
NM_001326309.2:c.1213C>G	NP_001313238.1:p.His405Asp
NM_001326310.2:c.2131C>G	NP_001313239.1:p.His711Asp
NM_001326311.2:c.1210C>G	NP_001313240.1:p.His404Asp
NM_001326312.2:c.2056C>G	NP_001313241.1:p.His686Asp
NM_001326313.2:c.1522C>G	NP_001313242.1:p.His508Asp
NM_001326314.2:c.1603C>G	NP_001313243.1:p.His535Asp
NM_001326315.2:c.2041C>G	NP_001313244.1:p.His681Asp
NM_207660.4:c.1675C>G	NP_997543.1:p.His559Asp
NM_207662.4:c.856C>G	NP_997545.2:p.His286Asp
NR_136936.2:n.2083C>G
NM_001326316.2:c.2041C>G	NP_001313245.1:p.His681Asp
NM_207661.3:c.1651C>G	NP_997544.1:p.His551Asp