Canonical Allele Identifier: CA487280453

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077252A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610908A>T , CM000676.2:g.88610908A>T	GRCh38
NC_000014.8:g.89077252A>T , CM000676.1:g.89077252A>T	GRCh37
NC_000014.7:g.88147005A>T	NCBI36
NG_050601.1:g.53000A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2172A>T MANE Select	ENSP00000251038.5:p.Arg724=
ENST00000649731.1:c.*1380A>T	ENSP00000497757.1:n.*1380A>T
ENST00000251038.9:c.2172A>T	ENSP00000251038.5:p.Arg724=
ENST00000302216.12:c.1701A>T	ENSP00000307025.8:p.Arg567=
ENST00000318308.10:c.882A>T	ENSP00000327176.6:p.Arg294=
ENST00000336693.8:c.1677A>T	ENSP00000338002.4:p.Arg559=
ENST00000393514.9:c.2097A>T	ENSP00000377150.5:p.Arg699=
ENST00000406216.7:c.810A>T	ENSP00000384682.3:p.Arg270=
ENST00000554020.5:n.1015A>T
ENST00000555755.5:c.2154A>T	ENSP00000452475.1:p.Arg718=
ENST00000555792.1:c.417A>T	ENSP00000450823.1:p.Arg139=
ENST00000555851.6:n.331A>T
ENST00000555900.5:c.1278A>T	ENSP00000451530.1:p.Arg426=
ENST00000556000.5:c.1916A>T
ENST00000556945.5:c.1779A>T	ENSP00000450474.1:p.Arg593=
ENST00000557491.1:n.1457A>T
ENST00000557607.5:c.1224A>T	ENSP00000452370.1:p.Arg408=
NM_001160103.1:c.2169A>T	NP_001153575.1:p.Arg723=
NM_001160104.1:c.2154A>T	NP_001153576.1:p.Arg718=
NM_024824.4:c.2172A>T	NP_079100.2:p.Arg724=
NM_207660.3:c.1701A>T	NP_997543.1:p.Arg567=
NM_207661.2:c.1677A>T	NP_997544.1:p.Arg559=
NM_207662.3:c.882A>T	NP_997545.2:p.Arg294=
XM_005268067.3:c.2157A>T	XP_005268124.1:p.Arg719=
XM_005268068.3:c.2097A>T	XP_005268125.1:p.Arg699=
XM_005268069.3:c.1779A>T	XP_005268126.1:p.Arg593=
XM_005268070.3:c.1776A>T	XP_005268127.1:p.Arg592=
XM_005268071.3:c.1704A>T	XP_005268128.1:p.Arg568=
XM_005268073.3:c.1278A>T	XP_005268130.1:p.Arg426=
XM_006720257.2:c.1203A>T	XP_006720320.1:p.Arg401=
XM_011537160.1:c.2070A>T	XP_011535462.1:p.Arg690=
XM_011537161.1:c.2016A>T	XP_011535463.1:p.Arg672=
NM_001326295.1:c.1779A>T	NP_001313224.1:p.Arg593=
NM_001326296.1:c.2094A>T	NP_001313225.1:p.Arg698=
NM_001326297.1:c.2070A>T	NP_001313226.1:p.Arg690=
NM_001326298.1:c.1704A>T	NP_001313227.1:p.Arg568=
NM_001326299.1:c.2079A>T	NP_001313228.1:p.Arg693=
NM_001326300.1:c.1707A>T	NP_001313229.1:p.Arg569=
NM_001326301.1:c.1995A>T	NP_001313230.1:p.Arg665=
NM_001326302.1:c.1704A>T	NP_001313231.1:p.Arg568=
NM_001326303.1:c.1599A>T	NP_001313232.1:p.Arg533=
NM_001326304.1:c.1311A>T	NP_001313233.1:p.Arg437=
NM_001326305.1:c.1632A>T	NP_001313234.1:p.Arg544=
NM_001326306.1:c.1545A>T	NP_001313235.1:p.Arg515=
NM_001326307.1:c.2097A>T	NP_001313236.1:p.Arg699=
NM_001326308.1:c.1314A>T	NP_001313237.1:p.Arg438=
NM_001326309.1:c.1239A>T	NP_001313238.1:p.Arg413=
NM_001326310.1:c.2157A>T	NP_001313239.1:p.Arg719=
NM_001326311.1:c.1236A>T	NP_001313240.1:p.Arg412=
NM_001326312.1:c.2082A>T	NP_001313241.1:p.Arg694=
NM_001326313.1:c.1548A>T	NP_001313242.1:p.Arg516=
NM_001326314.1:c.1629A>T	NP_001313243.1:p.Arg543=
NM_001326315.1:c.2067A>T	NP_001313244.1:p.Arg689=
NM_001326316.1:c.2067A>T	NP_001313245.1:p.Arg689=
NR_136936.1:n.2237A>T
XM_005268070.5:c.1776A>T	XP_005268127.1:p.Arg592=
XM_005268073.4:c.1278A>T	XP_005268130.1:p.Arg426=
XM_006720257.3:c.1203A>T	XP_006720320.1:p.Arg401=
XM_011537161.3:c.2016A>T	XP_011535463.1:p.Arg672=
XM_024449713.1:c.1200A>T	XP_024305481.1:p.Arg400=
NM_024824.5:c.2172A>T MANE Select	NP_079100.2:p.Arg724=
NM_001160103.2:c.2169A>T	NP_001153575.1:p.Arg723=
NM_001160104.2:c.2154A>T	NP_001153576.1:p.Arg718=
NM_001326295.2:c.1779A>T	NP_001313224.1:p.Arg593=
NM_001326296.2:c.2094A>T	NP_001313225.1:p.Arg698=
NM_001326297.2:c.2070A>T	NP_001313226.1:p.Arg690=
NM_001326298.2:c.1704A>T	NP_001313227.1:p.Arg568=
NM_001326299.2:c.2079A>T	NP_001313228.1:p.Arg693=
NM_001326300.2:c.1707A>T	NP_001313229.1:p.Arg569=
NM_001326301.2:c.1995A>T	NP_001313230.1:p.Arg665=
NM_001326302.2:c.1704A>T	NP_001313231.1:p.Arg568=
NM_001326303.2:c.1599A>T	NP_001313232.1:p.Arg533=
NM_001326304.2:c.1311A>T	NP_001313233.1:p.Arg437=
NM_001326305.2:c.1632A>T	NP_001313234.1:p.Arg544=
NM_001326306.2:c.1545A>T	NP_001313235.1:p.Arg515=
NM_001326307.2:c.2097A>T	NP_001313236.1:p.Arg699=
NM_001326308.2:c.1314A>T	NP_001313237.1:p.Arg438=
NM_001326309.2:c.1239A>T	NP_001313238.1:p.Arg413=
NM_001326310.2:c.2157A>T	NP_001313239.1:p.Arg719=
NM_001326311.2:c.1236A>T	NP_001313240.1:p.Arg412=
NM_001326312.2:c.2082A>T	NP_001313241.1:p.Arg694=
NM_001326313.2:c.1548A>T	NP_001313242.1:p.Arg516=
NM_001326314.2:c.1629A>T	NP_001313243.1:p.Arg543=
NM_001326315.2:c.2067A>T	NP_001313244.1:p.Arg689=
NM_207660.4:c.1701A>T	NP_997543.1:p.Arg567=
NM_207662.4:c.882A>T	NP_997545.2:p.Arg294=
NR_136936.2:n.2109A>T
NM_001326316.2:c.2067A>T	NP_001313245.1:p.Arg689=
NM_207661.3:c.1677A>T	NP_997544.1:p.Arg559=