Canonical Allele Identifier: CA390566124

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077236T>G (hg19) ; chr14:g.88610892T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610892T>G , CM000676.2:g.88610892T>G	GRCh38
NC_000014.8:g.89077236T>G , CM000676.1:g.89077236T>G	GRCh37
NC_000014.7:g.88146989T>G	NCBI36
NG_050601.1:g.52984T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2156T>G MANE Select	ENSP00000251038.5:p.Ile719Ser
ENST00000649731.1:c.*1364T>G	ENSP00000497757.1:n.*1364T>G
ENST00000251038.9:c.2156T>G	ENSP00000251038.5:p.Ile719Ser
ENST00000302216.12:c.1685T>G	ENSP00000307025.8:p.Ile562Ser
ENST00000318308.10:c.866T>G	ENSP00000327176.6:p.Ile289Ser
ENST00000336693.8:c.1661T>G	ENSP00000338002.4:p.Ile554Ser
ENST00000393514.9:c.2081T>G	ENSP00000377150.5:p.Ile694Ser
ENST00000406216.7:c.794T>G	ENSP00000384682.3:p.Ile265Ser
ENST00000554020.5:n.999T>G
ENST00000555755.5:c.2138T>G	ENSP00000452475.1:p.Ile713Ser
ENST00000555792.1:c.401T>G	ENSP00000450823.1:p.Ile134Ser
ENST00000555851.6:n.315T>G
ENST00000555900.5:c.1262T>G	ENSP00000451530.1:p.Ile421Ser
ENST00000556000.5:c.1900T>G
ENST00000556945.5:c.1763T>G	ENSP00000450474.1:p.Ile588Ser
ENST00000557491.1:n.1441T>G
ENST00000557607.5:c.1208T>G	ENSP00000452370.1:p.Ile403Ser
NM_001160103.1:c.2153T>G	NP_001153575.1:p.Ile718Ser
NM_001160104.1:c.2138T>G	NP_001153576.1:p.Ile713Ser
NM_024824.4:c.2156T>G	NP_079100.2:p.Ile719Ser
NM_207660.3:c.1685T>G	NP_997543.1:p.Ile562Ser
NM_207661.2:c.1661T>G	NP_997544.1:p.Ile554Ser
NM_207662.3:c.866T>G	NP_997545.2:p.Ile289Ser
XM_005268067.3:c.2141T>G	XP_005268124.1:p.Ile714Ser
XM_005268068.3:c.2081T>G	XP_005268125.1:p.Ile694Ser
XM_005268069.3:c.1763T>G	XP_005268126.1:p.Ile588Ser
XM_005268070.3:c.1760T>G	XP_005268127.1:p.Ile587Ser
XM_005268071.3:c.1688T>G	XP_005268128.1:p.Ile563Ser
XM_005268073.3:c.1262T>G	XP_005268130.1:p.Ile421Ser
XM_006720257.2:c.1187T>G	XP_006720320.1:p.Ile396Ser
XM_011537160.1:c.2054T>G	XP_011535462.1:p.Ile685Ser
XM_011537161.1:c.2000T>G	XP_011535463.1:p.Ile667Ser
NM_001326295.1:c.1763T>G	NP_001313224.1:p.Ile588Ser
NM_001326296.1:c.2078T>G	NP_001313225.1:p.Ile693Ser
NM_001326297.1:c.2054T>G	NP_001313226.1:p.Ile685Ser
NM_001326298.1:c.1688T>G	NP_001313227.1:p.Ile563Ser
NM_001326299.1:c.2063T>G	NP_001313228.1:p.Ile688Ser
NM_001326300.1:c.1691T>G	NP_001313229.1:p.Ile564Ser
NM_001326301.1:c.1979T>G	NP_001313230.1:p.Ile660Ser
NM_001326302.1:c.1688T>G	NP_001313231.1:p.Ile563Ser
NM_001326303.1:c.1583T>G	NP_001313232.1:p.Ile528Ser
NM_001326304.1:c.1295T>G	NP_001313233.1:p.Ile432Ser
NM_001326305.1:c.1616T>G	NP_001313234.1:p.Ile539Ser
NM_001326306.1:c.1529T>G	NP_001313235.1:p.Ile510Ser
NM_001326307.1:c.2081T>G	NP_001313236.1:p.Ile694Ser
NM_001326308.1:c.1298T>G	NP_001313237.1:p.Ile433Ser
NM_001326309.1:c.1223T>G	NP_001313238.1:p.Ile408Ser
NM_001326310.1:c.2141T>G	NP_001313239.1:p.Ile714Ser
NM_001326311.1:c.1220T>G	NP_001313240.1:p.Ile407Ser
NM_001326312.1:c.2066T>G	NP_001313241.1:p.Ile689Ser
NM_001326313.1:c.1532T>G	NP_001313242.1:p.Ile511Ser
NM_001326314.1:c.1613T>G	NP_001313243.1:p.Ile538Ser
NM_001326315.1:c.2051T>G	NP_001313244.1:p.Ile684Ser
NM_001326316.1:c.2051T>G	NP_001313245.1:p.Ile684Ser
NR_136936.1:n.2221T>G
XM_005268070.5:c.1760T>G	XP_005268127.1:p.Ile587Ser
XM_005268073.4:c.1262T>G	XP_005268130.1:p.Ile421Ser
XM_006720257.3:c.1187T>G	XP_006720320.1:p.Ile396Ser
XM_011537161.3:c.2000T>G	XP_011535463.1:p.Ile667Ser
XM_024449713.1:c.1184T>G	XP_024305481.1:p.Ile395Ser
NM_024824.5:c.2156T>G MANE Select	NP_079100.2:p.Ile719Ser
NM_001160103.2:c.2153T>G	NP_001153575.1:p.Ile718Ser
NM_001160104.2:c.2138T>G	NP_001153576.1:p.Ile713Ser
NM_001326295.2:c.1763T>G	NP_001313224.1:p.Ile588Ser
NM_001326296.2:c.2078T>G	NP_001313225.1:p.Ile693Ser
NM_001326297.2:c.2054T>G	NP_001313226.1:p.Ile685Ser
NM_001326298.2:c.1688T>G	NP_001313227.1:p.Ile563Ser
NM_001326299.2:c.2063T>G	NP_001313228.1:p.Ile688Ser
NM_001326300.2:c.1691T>G	NP_001313229.1:p.Ile564Ser
NM_001326301.2:c.1979T>G	NP_001313230.1:p.Ile660Ser
NM_001326302.2:c.1688T>G	NP_001313231.1:p.Ile563Ser
NM_001326303.2:c.1583T>G	NP_001313232.1:p.Ile528Ser
NM_001326304.2:c.1295T>G	NP_001313233.1:p.Ile432Ser
NM_001326305.2:c.1616T>G	NP_001313234.1:p.Ile539Ser
NM_001326306.2:c.1529T>G	NP_001313235.1:p.Ile510Ser
NM_001326307.2:c.2081T>G	NP_001313236.1:p.Ile694Ser
NM_001326308.2:c.1298T>G	NP_001313237.1:p.Ile433Ser
NM_001326309.2:c.1223T>G	NP_001313238.1:p.Ile408Ser
NM_001326310.2:c.2141T>G	NP_001313239.1:p.Ile714Ser
NM_001326311.2:c.1220T>G	NP_001313240.1:p.Ile407Ser
NM_001326312.2:c.2066T>G	NP_001313241.1:p.Ile689Ser
NM_001326313.2:c.1532T>G	NP_001313242.1:p.Ile511Ser
NM_001326314.2:c.1613T>G	NP_001313243.1:p.Ile538Ser
NM_001326315.2:c.2051T>G	NP_001313244.1:p.Ile684Ser
NM_207660.4:c.1685T>G	NP_997543.1:p.Ile562Ser
NM_207662.4:c.866T>G	NP_997545.2:p.Ile289Ser
NR_136936.2:n.2093T>G
NM_001326316.2:c.2051T>G	NP_001313245.1:p.Ile684Ser
NM_207661.3:c.1661T>G	NP_997544.1:p.Ile554Ser