Canonical Allele Identifier: CA487280416

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077204A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610860A>C , CM000676.2:g.88610860A>C	GRCh38
NC_000014.8:g.89077204A>C , CM000676.1:g.89077204A>C	GRCh37
NC_000014.7:g.88146957A>C	NCBI36
NG_050601.1:g.52952A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2124A>C MANE Select	ENSP00000251038.5:p.Thr708=
ENST00000649731.1:c.*1332A>C	ENSP00000497757.1:n.*1332A>C
ENST00000251038.9:c.2124A>C	ENSP00000251038.5:p.Thr708=
ENST00000302216.12:c.1653A>C	ENSP00000307025.8:p.Thr551=
ENST00000318308.10:c.834A>C	ENSP00000327176.6:p.Thr278=
ENST00000336693.8:c.1629A>C	ENSP00000338002.4:p.Thr543=
ENST00000393514.9:c.2049A>C	ENSP00000377150.5:p.Thr683=
ENST00000406216.7:c.762A>C	ENSP00000384682.3:p.Thr254=
ENST00000554020.5:n.967A>C
ENST00000555755.5:c.2106A>C	ENSP00000452475.1:p.Thr702=
ENST00000555792.1:c.369A>C	ENSP00000450823.1:p.Thr123=
ENST00000555851.6:n.283A>C
ENST00000555900.5:c.1230A>C	ENSP00000451530.1:p.Thr410=
ENST00000556000.5:c.1868A>C
ENST00000556945.5:c.1731A>C	ENSP00000450474.1:p.Thr577=
ENST00000557491.1:n.1409A>C
ENST00000557607.5:c.1176A>C	ENSP00000452370.1:p.Thr392=
NM_001160103.1:c.2121A>C	NP_001153575.1:p.Thr707=
NM_001160104.1:c.2106A>C	NP_001153576.1:p.Thr702=
NM_024824.4:c.2124A>C	NP_079100.2:p.Thr708=
NM_207660.3:c.1653A>C	NP_997543.1:p.Thr551=
NM_207661.2:c.1629A>C	NP_997544.1:p.Thr543=
NM_207662.3:c.834A>C	NP_997545.2:p.Thr278=
XM_005268067.3:c.2109A>C	XP_005268124.1:p.Thr703=
XM_005268068.3:c.2049A>C	XP_005268125.1:p.Thr683=
XM_005268069.3:c.1731A>C	XP_005268126.1:p.Thr577=
XM_005268070.3:c.1728A>C	XP_005268127.1:p.Thr576=
XM_005268071.3:c.1656A>C	XP_005268128.1:p.Thr552=
XM_005268073.3:c.1230A>C	XP_005268130.1:p.Thr410=
XM_006720257.2:c.1155A>C	XP_006720320.1:p.Thr385=
XM_011537160.1:c.2022A>C	XP_011535462.1:p.Thr674=
XM_011537161.1:c.1968A>C	XP_011535463.1:p.Thr656=
NM_001326295.1:c.1731A>C	NP_001313224.1:p.Thr577=
NM_001326296.1:c.2046A>C	NP_001313225.1:p.Thr682=
NM_001326297.1:c.2022A>C	NP_001313226.1:p.Thr674=
NM_001326298.1:c.1656A>C	NP_001313227.1:p.Thr552=
NM_001326299.1:c.2031A>C	NP_001313228.1:p.Thr677=
NM_001326300.1:c.1659A>C	NP_001313229.1:p.Thr553=
NM_001326301.1:c.1947A>C	NP_001313230.1:p.Thr649=
NM_001326302.1:c.1656A>C	NP_001313231.1:p.Thr552=
NM_001326303.1:c.1551A>C	NP_001313232.1:p.Thr517=
NM_001326304.1:c.1263A>C	NP_001313233.1:p.Thr421=
NM_001326305.1:c.1584A>C	NP_001313234.1:p.Thr528=
NM_001326306.1:c.1497A>C	NP_001313235.1:p.Thr499=
NM_001326307.1:c.2049A>C	NP_001313236.1:p.Thr683=
NM_001326308.1:c.1266A>C	NP_001313237.1:p.Thr422=
NM_001326309.1:c.1191A>C	NP_001313238.1:p.Thr397=
NM_001326310.1:c.2109A>C	NP_001313239.1:p.Thr703=
NM_001326311.1:c.1188A>C	NP_001313240.1:p.Thr396=
NM_001326312.1:c.2034A>C	NP_001313241.1:p.Thr678=
NM_001326313.1:c.1500A>C	NP_001313242.1:p.Thr500=
NM_001326314.1:c.1581A>C	NP_001313243.1:p.Thr527=
NM_001326315.1:c.2019A>C	NP_001313244.1:p.Thr673=
NM_001326316.1:c.2019A>C	NP_001313245.1:p.Thr673=
NR_136936.1:n.2189A>C
XM_005268070.5:c.1728A>C	XP_005268127.1:p.Thr576=
XM_005268073.4:c.1230A>C	XP_005268130.1:p.Thr410=
XM_006720257.3:c.1155A>C	XP_006720320.1:p.Thr385=
XM_011537161.3:c.1968A>C	XP_011535463.1:p.Thr656=
XM_024449713.1:c.1152A>C	XP_024305481.1:p.Thr384=
NM_024824.5:c.2124A>C MANE Select	NP_079100.2:p.Thr708=
NM_001160103.2:c.2121A>C	NP_001153575.1:p.Thr707=
NM_001160104.2:c.2106A>C	NP_001153576.1:p.Thr702=
NM_001326295.2:c.1731A>C	NP_001313224.1:p.Thr577=
NM_001326296.2:c.2046A>C	NP_001313225.1:p.Thr682=
NM_001326297.2:c.2022A>C	NP_001313226.1:p.Thr674=
NM_001326298.2:c.1656A>C	NP_001313227.1:p.Thr552=
NM_001326299.2:c.2031A>C	NP_001313228.1:p.Thr677=
NM_001326300.2:c.1659A>C	NP_001313229.1:p.Thr553=
NM_001326301.2:c.1947A>C	NP_001313230.1:p.Thr649=
NM_001326302.2:c.1656A>C	NP_001313231.1:p.Thr552=
NM_001326303.2:c.1551A>C	NP_001313232.1:p.Thr517=
NM_001326304.2:c.1263A>C	NP_001313233.1:p.Thr421=
NM_001326305.2:c.1584A>C	NP_001313234.1:p.Thr528=
NM_001326306.2:c.1497A>C	NP_001313235.1:p.Thr499=
NM_001326307.2:c.2049A>C	NP_001313236.1:p.Thr683=
NM_001326308.2:c.1266A>C	NP_001313237.1:p.Thr422=
NM_001326309.2:c.1191A>C	NP_001313238.1:p.Thr397=
NM_001326310.2:c.2109A>C	NP_001313239.1:p.Thr703=
NM_001326311.2:c.1188A>C	NP_001313240.1:p.Thr396=
NM_001326312.2:c.2034A>C	NP_001313241.1:p.Thr678=
NM_001326313.2:c.1500A>C	NP_001313242.1:p.Thr500=
NM_001326314.2:c.1581A>C	NP_001313243.1:p.Thr527=
NM_001326315.2:c.2019A>C	NP_001313244.1:p.Thr673=
NM_207660.4:c.1653A>C	NP_997543.1:p.Thr551=
NM_207662.4:c.834A>C	NP_997545.2:p.Thr278=
NR_136936.2:n.2061A>C
NM_001326316.2:c.2019A>C	NP_001313245.1:p.Thr673=
NM_207661.3:c.1629A>C	NP_997544.1:p.Thr543=