Canonical Allele Identifier: CA7300780

Gene: ZC3H14

Linked Data

• dbSNP Id: rs150624553
• ExAC: 14:89077203 C / T
• gnomAD v2: 14-89077203-C-T
• gnomAD v3: 14-88610859-C-T
• gnomAD v4: 14-88610859-C-T
• MyVariant Identifiers: chr14:g.89077203C>T (hg19) ; chr14:g.88610859C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610859C>T , CM000676.2:g.88610859C>T	GRCh38
NC_000014.8:g.89077203C>T , CM000676.1:g.89077203C>T	GRCh37
NC_000014.7:g.88146956C>T	NCBI36
NG_050601.1:g.52951C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2123C>T MANE Select	ENSP00000251038.5:p.Thr708Ile
ENST00000649731.1:c.*1331C>T	ENSP00000497757.1:n.*1331C>T
ENST00000251038.9:c.2123C>T	ENSP00000251038.5:p.Thr708Ile
ENST00000302216.12:c.1652C>T	ENSP00000307025.8:p.Thr551Ile
ENST00000318308.10:c.833C>T	ENSP00000327176.6:p.Thr278Ile
ENST00000336693.8:c.1628C>T	ENSP00000338002.4:p.Thr543Ile
ENST00000393514.9:c.2048C>T	ENSP00000377150.5:p.Thr683Ile
ENST00000406216.7:c.761C>T	ENSP00000384682.3:p.Thr254Ile
ENST00000554020.5:n.966C>T
ENST00000555755.5:c.2105C>T	ENSP00000452475.1:p.Thr702Ile
ENST00000555792.1:c.368C>T	ENSP00000450823.1:p.Thr123Ile
ENST00000555851.6:n.282C>T
ENST00000555900.5:c.1229C>T	ENSP00000451530.1:p.Thr410Ile
ENST00000556000.5:c.1867C>T
ENST00000556945.5:c.1730C>T	ENSP00000450474.1:p.Thr577Ile
ENST00000557491.1:n.1408C>T
ENST00000557607.5:c.1175C>T	ENSP00000452370.1:p.Thr392Ile
NM_001160103.1:c.2120C>T	NP_001153575.1:p.Thr707Ile
NM_001160104.1:c.2105C>T	NP_001153576.1:p.Thr702Ile
NM_024824.4:c.2123C>T	NP_079100.2:p.Thr708Ile
NM_207660.3:c.1652C>T	NP_997543.1:p.Thr551Ile
NM_207661.2:c.1628C>T	NP_997544.1:p.Thr543Ile
NM_207662.3:c.833C>T	NP_997545.2:p.Thr278Ile
XM_005268067.3:c.2108C>T	XP_005268124.1:p.Thr703Ile
XM_005268068.3:c.2048C>T	XP_005268125.1:p.Thr683Ile
XM_005268069.3:c.1730C>T	XP_005268126.1:p.Thr577Ile
XM_005268070.3:c.1727C>T	XP_005268127.1:p.Thr576Ile
XM_005268071.3:c.1655C>T	XP_005268128.1:p.Thr552Ile
XM_005268073.3:c.1229C>T	XP_005268130.1:p.Thr410Ile
XM_006720257.2:c.1154C>T	XP_006720320.1:p.Thr385Ile
XM_011537160.1:c.2021C>T	XP_011535462.1:p.Thr674Ile
XM_011537161.1:c.1967C>T	XP_011535463.1:p.Thr656Ile
NM_001326295.1:c.1730C>T	NP_001313224.1:p.Thr577Ile
NM_001326296.1:c.2045C>T	NP_001313225.1:p.Thr682Ile
NM_001326297.1:c.2021C>T	NP_001313226.1:p.Thr674Ile
NM_001326298.1:c.1655C>T	NP_001313227.1:p.Thr552Ile
NM_001326299.1:c.2030C>T	NP_001313228.1:p.Thr677Ile
NM_001326300.1:c.1658C>T	NP_001313229.1:p.Thr553Ile
NM_001326301.1:c.1946C>T	NP_001313230.1:p.Thr649Ile
NM_001326302.1:c.1655C>T	NP_001313231.1:p.Thr552Ile
NM_001326303.1:c.1550C>T	NP_001313232.1:p.Thr517Ile
NM_001326304.1:c.1262C>T	NP_001313233.1:p.Thr421Ile
NM_001326305.1:c.1583C>T	NP_001313234.1:p.Thr528Ile
NM_001326306.1:c.1496C>T	NP_001313235.1:p.Thr499Ile
NM_001326307.1:c.2048C>T	NP_001313236.1:p.Thr683Ile
NM_001326308.1:c.1265C>T	NP_001313237.1:p.Thr422Ile
NM_001326309.1:c.1190C>T	NP_001313238.1:p.Thr397Ile
NM_001326310.1:c.2108C>T	NP_001313239.1:p.Thr703Ile
NM_001326311.1:c.1187C>T	NP_001313240.1:p.Thr396Ile
NM_001326312.1:c.2033C>T	NP_001313241.1:p.Thr678Ile
NM_001326313.1:c.1499C>T	NP_001313242.1:p.Thr500Ile
NM_001326314.1:c.1580C>T	NP_001313243.1:p.Thr527Ile
NM_001326315.1:c.2018C>T	NP_001313244.1:p.Thr673Ile
NM_001326316.1:c.2018C>T	NP_001313245.1:p.Thr673Ile
NR_136936.1:n.2188C>T
XM_005268070.5:c.1727C>T	XP_005268127.1:p.Thr576Ile
XM_005268073.4:c.1229C>T	XP_005268130.1:p.Thr410Ile
XM_006720257.3:c.1154C>T	XP_006720320.1:p.Thr385Ile
XM_011537161.3:c.1967C>T	XP_011535463.1:p.Thr656Ile
XM_024449713.1:c.1151C>T	XP_024305481.1:p.Thr384Ile
NM_024824.5:c.2123C>T MANE Select	NP_079100.2:p.Thr708Ile
NM_001160103.2:c.2120C>T	NP_001153575.1:p.Thr707Ile
NM_001160104.2:c.2105C>T	NP_001153576.1:p.Thr702Ile
NM_001326295.2:c.1730C>T	NP_001313224.1:p.Thr577Ile
NM_001326296.2:c.2045C>T	NP_001313225.1:p.Thr682Ile
NM_001326297.2:c.2021C>T	NP_001313226.1:p.Thr674Ile
NM_001326298.2:c.1655C>T	NP_001313227.1:p.Thr552Ile
NM_001326299.2:c.2030C>T	NP_001313228.1:p.Thr677Ile
NM_001326300.2:c.1658C>T	NP_001313229.1:p.Thr553Ile
NM_001326301.2:c.1946C>T	NP_001313230.1:p.Thr649Ile
NM_001326302.2:c.1655C>T	NP_001313231.1:p.Thr552Ile
NM_001326303.2:c.1550C>T	NP_001313232.1:p.Thr517Ile
NM_001326304.2:c.1262C>T	NP_001313233.1:p.Thr421Ile
NM_001326305.2:c.1583C>T	NP_001313234.1:p.Thr528Ile
NM_001326306.2:c.1496C>T	NP_001313235.1:p.Thr499Ile
NM_001326307.2:c.2048C>T	NP_001313236.1:p.Thr683Ile
NM_001326308.2:c.1265C>T	NP_001313237.1:p.Thr422Ile
NM_001326309.2:c.1190C>T	NP_001313238.1:p.Thr397Ile
NM_001326310.2:c.2108C>T	NP_001313239.1:p.Thr703Ile
NM_001326311.2:c.1187C>T	NP_001313240.1:p.Thr396Ile
NM_001326312.2:c.2033C>T	NP_001313241.1:p.Thr678Ile
NM_001326313.2:c.1499C>T	NP_001313242.1:p.Thr500Ile
NM_001326314.2:c.1580C>T	NP_001313243.1:p.Thr527Ile
NM_001326315.2:c.2018C>T	NP_001313244.1:p.Thr673Ile
NM_207660.4:c.1652C>T	NP_997543.1:p.Thr551Ile
NM_207662.4:c.833C>T	NP_997545.2:p.Thr278Ile
NR_136936.2:n.2060C>T
NM_001326316.2:c.2018C>T	NP_001313245.1:p.Thr673Ile
NM_207661.3:c.1628C>T	NP_997544.1:p.Thr543Ile