Canonical Allele Identifier: CA390565964

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077218C>G (hg19) ; chr14:g.88610874C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610874C>G , CM000676.2:g.88610874C>G	GRCh38
NC_000014.8:g.89077218C>G , CM000676.1:g.89077218C>G	GRCh37
NC_000014.7:g.88146971C>G	NCBI36
NG_050601.1:g.52966C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2138C>G MANE Select	ENSP00000251038.5:p.Thr713Arg
ENST00000649731.1:c.*1346C>G	ENSP00000497757.1:n.*1346C>G
ENST00000251038.9:c.2138C>G	ENSP00000251038.5:p.Thr713Arg
ENST00000302216.12:c.1667C>G	ENSP00000307025.8:p.Thr556Arg
ENST00000318308.10:c.848C>G	ENSP00000327176.6:p.Thr283Arg
ENST00000336693.8:c.1643C>G	ENSP00000338002.4:p.Thr548Arg
ENST00000393514.9:c.2063C>G	ENSP00000377150.5:p.Thr688Arg
ENST00000406216.7:c.776C>G	ENSP00000384682.3:p.Thr259Arg
ENST00000554020.5:n.981C>G
ENST00000555755.5:c.2120C>G	ENSP00000452475.1:p.Thr707Arg
ENST00000555792.1:c.383C>G	ENSP00000450823.1:p.Thr128Arg
ENST00000555851.6:n.297C>G
ENST00000555900.5:c.1244C>G	ENSP00000451530.1:p.Thr415Arg
ENST00000556000.5:c.1882C>G
ENST00000556945.5:c.1745C>G	ENSP00000450474.1:p.Thr582Arg
ENST00000557491.1:n.1423C>G
ENST00000557607.5:c.1190C>G	ENSP00000452370.1:p.Thr397Arg
NM_001160103.1:c.2135C>G	NP_001153575.1:p.Thr712Arg
NM_001160104.1:c.2120C>G	NP_001153576.1:p.Thr707Arg
NM_024824.4:c.2138C>G	NP_079100.2:p.Thr713Arg
NM_207660.3:c.1667C>G	NP_997543.1:p.Thr556Arg
NM_207661.2:c.1643C>G	NP_997544.1:p.Thr548Arg
NM_207662.3:c.848C>G	NP_997545.2:p.Thr283Arg
XM_005268067.3:c.2123C>G	XP_005268124.1:p.Thr708Arg
XM_005268068.3:c.2063C>G	XP_005268125.1:p.Thr688Arg
XM_005268069.3:c.1745C>G	XP_005268126.1:p.Thr582Arg
XM_005268070.3:c.1742C>G	XP_005268127.1:p.Thr581Arg
XM_005268071.3:c.1670C>G	XP_005268128.1:p.Thr557Arg
XM_005268073.3:c.1244C>G	XP_005268130.1:p.Thr415Arg
XM_006720257.2:c.1169C>G	XP_006720320.1:p.Thr390Arg
XM_011537160.1:c.2036C>G	XP_011535462.1:p.Thr679Arg
XM_011537161.1:c.1982C>G	XP_011535463.1:p.Thr661Arg
NM_001326295.1:c.1745C>G	NP_001313224.1:p.Thr582Arg
NM_001326296.1:c.2060C>G	NP_001313225.1:p.Thr687Arg
NM_001326297.1:c.2036C>G	NP_001313226.1:p.Thr679Arg
NM_001326298.1:c.1670C>G	NP_001313227.1:p.Thr557Arg
NM_001326299.1:c.2045C>G	NP_001313228.1:p.Thr682Arg
NM_001326300.1:c.1673C>G	NP_001313229.1:p.Thr558Arg
NM_001326301.1:c.1961C>G	NP_001313230.1:p.Thr654Arg
NM_001326302.1:c.1670C>G	NP_001313231.1:p.Thr557Arg
NM_001326303.1:c.1565C>G	NP_001313232.1:p.Thr522Arg
NM_001326304.1:c.1277C>G	NP_001313233.1:p.Thr426Arg
NM_001326305.1:c.1598C>G	NP_001313234.1:p.Thr533Arg
NM_001326306.1:c.1511C>G	NP_001313235.1:p.Thr504Arg
NM_001326307.1:c.2063C>G	NP_001313236.1:p.Thr688Arg
NM_001326308.1:c.1280C>G	NP_001313237.1:p.Thr427Arg
NM_001326309.1:c.1205C>G	NP_001313238.1:p.Thr402Arg
NM_001326310.1:c.2123C>G	NP_001313239.1:p.Thr708Arg
NM_001326311.1:c.1202C>G	NP_001313240.1:p.Thr401Arg
NM_001326312.1:c.2048C>G	NP_001313241.1:p.Thr683Arg
NM_001326313.1:c.1514C>G	NP_001313242.1:p.Thr505Arg
NM_001326314.1:c.1595C>G	NP_001313243.1:p.Thr532Arg
NM_001326315.1:c.2033C>G	NP_001313244.1:p.Thr678Arg
NM_001326316.1:c.2033C>G	NP_001313245.1:p.Thr678Arg
NR_136936.1:n.2203C>G
XM_005268070.5:c.1742C>G	XP_005268127.1:p.Thr581Arg
XM_005268073.4:c.1244C>G	XP_005268130.1:p.Thr415Arg
XM_006720257.3:c.1169C>G	XP_006720320.1:p.Thr390Arg
XM_011537161.3:c.1982C>G	XP_011535463.1:p.Thr661Arg
XM_024449713.1:c.1166C>G	XP_024305481.1:p.Thr389Arg
NM_024824.5:c.2138C>G MANE Select	NP_079100.2:p.Thr713Arg
NM_001160103.2:c.2135C>G	NP_001153575.1:p.Thr712Arg
NM_001160104.2:c.2120C>G	NP_001153576.1:p.Thr707Arg
NM_001326295.2:c.1745C>G	NP_001313224.1:p.Thr582Arg
NM_001326296.2:c.2060C>G	NP_001313225.1:p.Thr687Arg
NM_001326297.2:c.2036C>G	NP_001313226.1:p.Thr679Arg
NM_001326298.2:c.1670C>G	NP_001313227.1:p.Thr557Arg
NM_001326299.2:c.2045C>G	NP_001313228.1:p.Thr682Arg
NM_001326300.2:c.1673C>G	NP_001313229.1:p.Thr558Arg
NM_001326301.2:c.1961C>G	NP_001313230.1:p.Thr654Arg
NM_001326302.2:c.1670C>G	NP_001313231.1:p.Thr557Arg
NM_001326303.2:c.1565C>G	NP_001313232.1:p.Thr522Arg
NM_001326304.2:c.1277C>G	NP_001313233.1:p.Thr426Arg
NM_001326305.2:c.1598C>G	NP_001313234.1:p.Thr533Arg
NM_001326306.2:c.1511C>G	NP_001313235.1:p.Thr504Arg
NM_001326307.2:c.2063C>G	NP_001313236.1:p.Thr688Arg
NM_001326308.2:c.1280C>G	NP_001313237.1:p.Thr427Arg
NM_001326309.2:c.1205C>G	NP_001313238.1:p.Thr402Arg
NM_001326310.2:c.2123C>G	NP_001313239.1:p.Thr708Arg
NM_001326311.2:c.1202C>G	NP_001313240.1:p.Thr401Arg
NM_001326312.2:c.2048C>G	NP_001313241.1:p.Thr683Arg
NM_001326313.2:c.1514C>G	NP_001313242.1:p.Thr505Arg
NM_001326314.2:c.1595C>G	NP_001313243.1:p.Thr532Arg
NM_001326315.2:c.2033C>G	NP_001313244.1:p.Thr678Arg
NM_207660.4:c.1667C>G	NP_997543.1:p.Thr556Arg
NM_207662.4:c.848C>G	NP_997545.2:p.Thr283Arg
NR_136936.2:n.2075C>G
NM_001326316.2:c.2033C>G	NP_001313245.1:p.Thr678Arg
NM_207661.3:c.1643C>G	NP_997544.1:p.Thr548Arg