Canonical Allele Identifier: CA390565764

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077201T>G (hg19) ; chr14:g.88610857T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610857T>G , CM000676.2:g.88610857T>G	GRCh38
NC_000014.8:g.89077201T>G , CM000676.1:g.89077201T>G	GRCh37
NC_000014.7:g.88146954T>G	NCBI36
NG_050601.1:g.52949T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2121T>G MANE Select	ENSP00000251038.5:p.Cys707Trp
ENST00000649731.1:c.*1329T>G	ENSP00000497757.1:n.*1329T>G
ENST00000251038.9:c.2121T>G	ENSP00000251038.5:p.Cys707Trp
ENST00000302216.12:c.1650T>G	ENSP00000307025.8:p.Cys550Trp
ENST00000318308.10:c.831T>G	ENSP00000327176.6:p.Cys277Trp
ENST00000336693.8:c.1626T>G	ENSP00000338002.4:p.Cys542Trp
ENST00000393514.9:c.2046T>G	ENSP00000377150.5:p.Cys682Trp
ENST00000406216.7:c.759T>G	ENSP00000384682.3:p.Cys253Trp
ENST00000554020.5:n.964T>G
ENST00000555755.5:c.2103T>G	ENSP00000452475.1:p.Cys701Trp
ENST00000555792.1:c.366T>G	ENSP00000450823.1:p.Cys122Trp
ENST00000555851.6:n.280T>G
ENST00000555900.5:c.1227T>G	ENSP00000451530.1:p.Cys409Trp
ENST00000556000.5:c.1865T>G
ENST00000556945.5:c.1728T>G	ENSP00000450474.1:p.Cys576Trp
ENST00000557491.1:n.1406T>G
ENST00000557607.5:c.1173T>G	ENSP00000452370.1:p.Cys391Trp
NM_001160103.1:c.2118T>G	NP_001153575.1:p.Cys706Trp
NM_001160104.1:c.2103T>G	NP_001153576.1:p.Cys701Trp
NM_024824.4:c.2121T>G	NP_079100.2:p.Cys707Trp
NM_207660.3:c.1650T>G	NP_997543.1:p.Cys550Trp
NM_207661.2:c.1626T>G	NP_997544.1:p.Cys542Trp
NM_207662.3:c.831T>G	NP_997545.2:p.Cys277Trp
XM_005268067.3:c.2106T>G	XP_005268124.1:p.Cys702Trp
XM_005268068.3:c.2046T>G	XP_005268125.1:p.Cys682Trp
XM_005268069.3:c.1728T>G	XP_005268126.1:p.Cys576Trp
XM_005268070.3:c.1725T>G	XP_005268127.1:p.Cys575Trp
XM_005268071.3:c.1653T>G	XP_005268128.1:p.Cys551Trp
XM_005268073.3:c.1227T>G	XP_005268130.1:p.Cys409Trp
XM_006720257.2:c.1152T>G	XP_006720320.1:p.Cys384Trp
XM_011537160.1:c.2019T>G	XP_011535462.1:p.Cys673Trp
XM_011537161.1:c.1965T>G	XP_011535463.1:p.Cys655Trp
NM_001326295.1:c.1728T>G	NP_001313224.1:p.Cys576Trp
NM_001326296.1:c.2043T>G	NP_001313225.1:p.Cys681Trp
NM_001326297.1:c.2019T>G	NP_001313226.1:p.Cys673Trp
NM_001326298.1:c.1653T>G	NP_001313227.1:p.Cys551Trp
NM_001326299.1:c.2028T>G	NP_001313228.1:p.Cys676Trp
NM_001326300.1:c.1656T>G	NP_001313229.1:p.Cys552Trp
NM_001326301.1:c.1944T>G	NP_001313230.1:p.Cys648Trp
NM_001326302.1:c.1653T>G	NP_001313231.1:p.Cys551Trp
NM_001326303.1:c.1548T>G	NP_001313232.1:p.Cys516Trp
NM_001326304.1:c.1260T>G	NP_001313233.1:p.Cys420Trp
NM_001326305.1:c.1581T>G	NP_001313234.1:p.Cys527Trp
NM_001326306.1:c.1494T>G	NP_001313235.1:p.Cys498Trp
NM_001326307.1:c.2046T>G	NP_001313236.1:p.Cys682Trp
NM_001326308.1:c.1263T>G	NP_001313237.1:p.Cys421Trp
NM_001326309.1:c.1188T>G	NP_001313238.1:p.Cys396Trp
NM_001326310.1:c.2106T>G	NP_001313239.1:p.Cys702Trp
NM_001326311.1:c.1185T>G	NP_001313240.1:p.Cys395Trp
NM_001326312.1:c.2031T>G	NP_001313241.1:p.Cys677Trp
NM_001326313.1:c.1497T>G	NP_001313242.1:p.Cys499Trp
NM_001326314.1:c.1578T>G	NP_001313243.1:p.Cys526Trp
NM_001326315.1:c.2016T>G	NP_001313244.1:p.Cys672Trp
NM_001326316.1:c.2016T>G	NP_001313245.1:p.Cys672Trp
NR_136936.1:n.2186T>G
XM_005268070.5:c.1725T>G	XP_005268127.1:p.Cys575Trp
XM_005268073.4:c.1227T>G	XP_005268130.1:p.Cys409Trp
XM_006720257.3:c.1152T>G	XP_006720320.1:p.Cys384Trp
XM_011537161.3:c.1965T>G	XP_011535463.1:p.Cys655Trp
XM_024449713.1:c.1149T>G	XP_024305481.1:p.Cys383Trp
NM_024824.5:c.2121T>G MANE Select	NP_079100.2:p.Cys707Trp
NM_001160103.2:c.2118T>G	NP_001153575.1:p.Cys706Trp
NM_001160104.2:c.2103T>G	NP_001153576.1:p.Cys701Trp
NM_001326295.2:c.1728T>G	NP_001313224.1:p.Cys576Trp
NM_001326296.2:c.2043T>G	NP_001313225.1:p.Cys681Trp
NM_001326297.2:c.2019T>G	NP_001313226.1:p.Cys673Trp
NM_001326298.2:c.1653T>G	NP_001313227.1:p.Cys551Trp
NM_001326299.2:c.2028T>G	NP_001313228.1:p.Cys676Trp
NM_001326300.2:c.1656T>G	NP_001313229.1:p.Cys552Trp
NM_001326301.2:c.1944T>G	NP_001313230.1:p.Cys648Trp
NM_001326302.2:c.1653T>G	NP_001313231.1:p.Cys551Trp
NM_001326303.2:c.1548T>G	NP_001313232.1:p.Cys516Trp
NM_001326304.2:c.1260T>G	NP_001313233.1:p.Cys420Trp
NM_001326305.2:c.1581T>G	NP_001313234.1:p.Cys527Trp
NM_001326306.2:c.1494T>G	NP_001313235.1:p.Cys498Trp
NM_001326307.2:c.2046T>G	NP_001313236.1:p.Cys682Trp
NM_001326308.2:c.1263T>G	NP_001313237.1:p.Cys421Trp
NM_001326309.2:c.1188T>G	NP_001313238.1:p.Cys396Trp
NM_001326310.2:c.2106T>G	NP_001313239.1:p.Cys702Trp
NM_001326311.2:c.1185T>G	NP_001313240.1:p.Cys395Trp
NM_001326312.2:c.2031T>G	NP_001313241.1:p.Cys677Trp
NM_001326313.2:c.1497T>G	NP_001313242.1:p.Cys499Trp
NM_001326314.2:c.1578T>G	NP_001313243.1:p.Cys526Trp
NM_001326315.2:c.2016T>G	NP_001313244.1:p.Cys672Trp
NM_207660.4:c.1650T>G	NP_997543.1:p.Cys550Trp
NM_207662.4:c.831T>G	NP_997545.2:p.Cys277Trp
NR_136936.2:n.2058T>G
NM_001326316.2:c.2016T>G	NP_001313245.1:p.Cys672Trp
NM_207661.3:c.1626T>G	NP_997544.1:p.Cys542Trp