Canonical Allele Identifier: CA390566402

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077270T>G (hg19) ; chr14:g.88610926T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610926T>G , CM000676.2:g.88610926T>G	GRCh38
NC_000014.8:g.89077270T>G , CM000676.1:g.89077270T>G	GRCh37
NC_000014.7:g.88147023T>G	NCBI36
NG_050601.1:g.53018T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2190T>G MANE Select	ENSP00000251038.5:p.Ile730Met
ENST00000649731.1:c.*1398T>G	ENSP00000497757.1:n.*1398T>G
ENST00000251038.9:c.2190T>G	ENSP00000251038.5:p.Ile730Met
ENST00000302216.12:c.1719T>G	ENSP00000307025.8:p.Ile573Met
ENST00000318308.10:c.900T>G	ENSP00000327176.6:p.Ile300Met
ENST00000336693.8:c.1695T>G	ENSP00000338002.4:p.Ile565Met
ENST00000393514.9:c.2115T>G	ENSP00000377150.5:p.Ile705Met
ENST00000406216.7:c.828T>G	ENSP00000384682.3:p.Ile276Met
ENST00000554020.5:n.1033T>G
ENST00000555755.5:c.2172T>G	ENSP00000452475.1:p.Ile724Met
ENST00000555792.1:c.435T>G	ENSP00000450823.1:p.Ile145Met
ENST00000555851.6:n.349T>G
ENST00000555900.5:c.1296T>G	ENSP00000451530.1:p.Ile432Met
ENST00000556000.5:c.1934T>G
ENST00000556945.5:c.1797T>G	ENSP00000450474.1:p.Ile599Met
ENST00000557491.1:n.1475T>G
ENST00000557607.5:c.1242T>G	ENSP00000452370.1:p.Ile414Met
NM_001160103.1:c.2187T>G	NP_001153575.1:p.Ile729Met
NM_001160104.1:c.2172T>G	NP_001153576.1:p.Ile724Met
NM_024824.4:c.2190T>G	NP_079100.2:p.Ile730Met
NM_207660.3:c.1719T>G	NP_997543.1:p.Ile573Met
NM_207661.2:c.1695T>G	NP_997544.1:p.Ile565Met
NM_207662.3:c.900T>G	NP_997545.2:p.Ile300Met
XM_005268067.3:c.2175T>G	XP_005268124.1:p.Ile725Met
XM_005268068.3:c.2115T>G	XP_005268125.1:p.Ile705Met
XM_005268069.3:c.1797T>G	XP_005268126.1:p.Ile599Met
XM_005268070.3:c.1794T>G	XP_005268127.1:p.Ile598Met
XM_005268071.3:c.1722T>G	XP_005268128.1:p.Ile574Met
XM_005268073.3:c.1296T>G	XP_005268130.1:p.Ile432Met
XM_006720257.2:c.1221T>G	XP_006720320.1:p.Ile407Met
XM_011537160.1:c.2088T>G	XP_011535462.1:p.Ile696Met
XM_011537161.1:c.2034T>G	XP_011535463.1:p.Ile678Met
NM_001326295.1:c.1797T>G	NP_001313224.1:p.Ile599Met
NM_001326296.1:c.2112T>G	NP_001313225.1:p.Ile704Met
NM_001326297.1:c.2088T>G	NP_001313226.1:p.Ile696Met
NM_001326298.1:c.1722T>G	NP_001313227.1:p.Ile574Met
NM_001326299.1:c.2097T>G	NP_001313228.1:p.Ile699Met
NM_001326300.1:c.1725T>G	NP_001313229.1:p.Ile575Met
NM_001326301.1:c.2013T>G	NP_001313230.1:p.Ile671Met
NM_001326302.1:c.1722T>G	NP_001313231.1:p.Ile574Met
NM_001326303.1:c.1617T>G	NP_001313232.1:p.Ile539Met
NM_001326304.1:c.1329T>G	NP_001313233.1:p.Ile443Met
NM_001326305.1:c.1650T>G	NP_001313234.1:p.Ile550Met
NM_001326306.1:c.1563T>G	NP_001313235.1:p.Ile521Met
NM_001326307.1:c.2115T>G	NP_001313236.1:p.Ile705Met
NM_001326308.1:c.1332T>G	NP_001313237.1:p.Ile444Met
NM_001326309.1:c.1257T>G	NP_001313238.1:p.Ile419Met
NM_001326310.1:c.2175T>G	NP_001313239.1:p.Ile725Met
NM_001326311.1:c.1254T>G	NP_001313240.1:p.Ile418Met
NM_001326312.1:c.2100T>G	NP_001313241.1:p.Ile700Met
NM_001326313.1:c.1566T>G	NP_001313242.1:p.Ile522Met
NM_001326314.1:c.1647T>G	NP_001313243.1:p.Ile549Met
NM_001326315.1:c.2085T>G	NP_001313244.1:p.Ile695Met
NM_001326316.1:c.2085T>G	NP_001313245.1:p.Ile695Met
NR_136936.1:n.2255T>G
XM_005268070.5:c.1794T>G	XP_005268127.1:p.Ile598Met
XM_005268073.4:c.1296T>G	XP_005268130.1:p.Ile432Met
XM_006720257.3:c.1221T>G	XP_006720320.1:p.Ile407Met
XM_011537161.3:c.2034T>G	XP_011535463.1:p.Ile678Met
XM_024449713.1:c.1218T>G	XP_024305481.1:p.Ile406Met
NM_024824.5:c.2190T>G MANE Select	NP_079100.2:p.Ile730Met
NM_001160103.2:c.2187T>G	NP_001153575.1:p.Ile729Met
NM_001160104.2:c.2172T>G	NP_001153576.1:p.Ile724Met
NM_001326295.2:c.1797T>G	NP_001313224.1:p.Ile599Met
NM_001326296.2:c.2112T>G	NP_001313225.1:p.Ile704Met
NM_001326297.2:c.2088T>G	NP_001313226.1:p.Ile696Met
NM_001326298.2:c.1722T>G	NP_001313227.1:p.Ile574Met
NM_001326299.2:c.2097T>G	NP_001313228.1:p.Ile699Met
NM_001326300.2:c.1725T>G	NP_001313229.1:p.Ile575Met
NM_001326301.2:c.2013T>G	NP_001313230.1:p.Ile671Met
NM_001326302.2:c.1722T>G	NP_001313231.1:p.Ile574Met
NM_001326303.2:c.1617T>G	NP_001313232.1:p.Ile539Met
NM_001326304.2:c.1329T>G	NP_001313233.1:p.Ile443Met
NM_001326305.2:c.1650T>G	NP_001313234.1:p.Ile550Met
NM_001326306.2:c.1563T>G	NP_001313235.1:p.Ile521Met
NM_001326307.2:c.2115T>G	NP_001313236.1:p.Ile705Met
NM_001326308.2:c.1332T>G	NP_001313237.1:p.Ile444Met
NM_001326309.2:c.1257T>G	NP_001313238.1:p.Ile419Met
NM_001326310.2:c.2175T>G	NP_001313239.1:p.Ile725Met
NM_001326311.2:c.1254T>G	NP_001313240.1:p.Ile418Met
NM_001326312.2:c.2100T>G	NP_001313241.1:p.Ile700Met
NM_001326313.2:c.1566T>G	NP_001313242.1:p.Ile522Met
NM_001326314.2:c.1647T>G	NP_001313243.1:p.Ile549Met
NM_001326315.2:c.2085T>G	NP_001313244.1:p.Ile695Met
NM_207660.4:c.1719T>G	NP_997543.1:p.Ile573Met
NM_207662.4:c.900T>G	NP_997545.2:p.Ile300Met
NR_136936.2:n.2127T>G
NM_001326316.2:c.2085T>G	NP_001313245.1:p.Ile695Met
NM_207661.3:c.1695T>G	NP_997544.1:p.Ile565Met