Canonical Allele Identifier: CA487280431

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077228T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610884T>C , CM000676.2:g.88610884T>C	GRCh38
NC_000014.8:g.89077228T>C , CM000676.1:g.89077228T>C	GRCh37
NC_000014.7:g.88146981T>C	NCBI36
NG_050601.1:g.52976T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2148T>C MANE Select	ENSP00000251038.5:p.His716=
ENST00000649731.1:c.*1356T>C	ENSP00000497757.1:n.*1356T>C
ENST00000251038.9:c.2148T>C	ENSP00000251038.5:p.His716=
ENST00000302216.12:c.1677T>C	ENSP00000307025.8:p.His559=
ENST00000318308.10:c.858T>C	ENSP00000327176.6:p.His286=
ENST00000336693.8:c.1653T>C	ENSP00000338002.4:p.His551=
ENST00000393514.9:c.2073T>C	ENSP00000377150.5:p.His691=
ENST00000406216.7:c.786T>C	ENSP00000384682.3:p.His262=
ENST00000554020.5:n.991T>C
ENST00000555755.5:c.2130T>C	ENSP00000452475.1:p.His710=
ENST00000555792.1:c.393T>C	ENSP00000450823.1:p.His131=
ENST00000555851.6:n.307T>C
ENST00000555900.5:c.1254T>C	ENSP00000451530.1:p.His418=
ENST00000556000.5:c.1892T>C
ENST00000556945.5:c.1755T>C	ENSP00000450474.1:p.His585=
ENST00000557491.1:n.1433T>C
ENST00000557607.5:c.1200T>C	ENSP00000452370.1:p.His400=
NM_001160103.1:c.2145T>C	NP_001153575.1:p.His715=
NM_001160104.1:c.2130T>C	NP_001153576.1:p.His710=
NM_024824.4:c.2148T>C	NP_079100.2:p.His716=
NM_207660.3:c.1677T>C	NP_997543.1:p.His559=
NM_207661.2:c.1653T>C	NP_997544.1:p.His551=
NM_207662.3:c.858T>C	NP_997545.2:p.His286=
XM_005268067.3:c.2133T>C	XP_005268124.1:p.His711=
XM_005268068.3:c.2073T>C	XP_005268125.1:p.His691=
XM_005268069.3:c.1755T>C	XP_005268126.1:p.His585=
XM_005268070.3:c.1752T>C	XP_005268127.1:p.His584=
XM_005268071.3:c.1680T>C	XP_005268128.1:p.His560=
XM_005268073.3:c.1254T>C	XP_005268130.1:p.His418=
XM_006720257.2:c.1179T>C	XP_006720320.1:p.His393=
XM_011537160.1:c.2046T>C	XP_011535462.1:p.His682=
XM_011537161.1:c.1992T>C	XP_011535463.1:p.His664=
NM_001326295.1:c.1755T>C	NP_001313224.1:p.His585=
NM_001326296.1:c.2070T>C	NP_001313225.1:p.His690=
NM_001326297.1:c.2046T>C	NP_001313226.1:p.His682=
NM_001326298.1:c.1680T>C	NP_001313227.1:p.His560=
NM_001326299.1:c.2055T>C	NP_001313228.1:p.His685=
NM_001326300.1:c.1683T>C	NP_001313229.1:p.His561=
NM_001326301.1:c.1971T>C	NP_001313230.1:p.His657=
NM_001326302.1:c.1680T>C	NP_001313231.1:p.His560=
NM_001326303.1:c.1575T>C	NP_001313232.1:p.His525=
NM_001326304.1:c.1287T>C	NP_001313233.1:p.His429=
NM_001326305.1:c.1608T>C	NP_001313234.1:p.His536=
NM_001326306.1:c.1521T>C	NP_001313235.1:p.His507=
NM_001326307.1:c.2073T>C	NP_001313236.1:p.His691=
NM_001326308.1:c.1290T>C	NP_001313237.1:p.His430=
NM_001326309.1:c.1215T>C	NP_001313238.1:p.His405=
NM_001326310.1:c.2133T>C	NP_001313239.1:p.His711=
NM_001326311.1:c.1212T>C	NP_001313240.1:p.His404=
NM_001326312.1:c.2058T>C	NP_001313241.1:p.His686=
NM_001326313.1:c.1524T>C	NP_001313242.1:p.His508=
NM_001326314.1:c.1605T>C	NP_001313243.1:p.His535=
NM_001326315.1:c.2043T>C	NP_001313244.1:p.His681=
NM_001326316.1:c.2043T>C	NP_001313245.1:p.His681=
NR_136936.1:n.2213T>C
XM_005268070.5:c.1752T>C	XP_005268127.1:p.His584=
XM_005268073.4:c.1254T>C	XP_005268130.1:p.His418=
XM_006720257.3:c.1179T>C	XP_006720320.1:p.His393=
XM_011537161.3:c.1992T>C	XP_011535463.1:p.His664=
XM_024449713.1:c.1176T>C	XP_024305481.1:p.His392=
NM_024824.5:c.2148T>C MANE Select	NP_079100.2:p.His716=
NM_001160103.2:c.2145T>C	NP_001153575.1:p.His715=
NM_001160104.2:c.2130T>C	NP_001153576.1:p.His710=
NM_001326295.2:c.1755T>C	NP_001313224.1:p.His585=
NM_001326296.2:c.2070T>C	NP_001313225.1:p.His690=
NM_001326297.2:c.2046T>C	NP_001313226.1:p.His682=
NM_001326298.2:c.1680T>C	NP_001313227.1:p.His560=
NM_001326299.2:c.2055T>C	NP_001313228.1:p.His685=
NM_001326300.2:c.1683T>C	NP_001313229.1:p.His561=
NM_001326301.2:c.1971T>C	NP_001313230.1:p.His657=
NM_001326302.2:c.1680T>C	NP_001313231.1:p.His560=
NM_001326303.2:c.1575T>C	NP_001313232.1:p.His525=
NM_001326304.2:c.1287T>C	NP_001313233.1:p.His429=
NM_001326305.2:c.1608T>C	NP_001313234.1:p.His536=
NM_001326306.2:c.1521T>C	NP_001313235.1:p.His507=
NM_001326307.2:c.2073T>C	NP_001313236.1:p.His691=
NM_001326308.2:c.1290T>C	NP_001313237.1:p.His430=
NM_001326309.2:c.1215T>C	NP_001313238.1:p.His405=
NM_001326310.2:c.2133T>C	NP_001313239.1:p.His711=
NM_001326311.2:c.1212T>C	NP_001313240.1:p.His404=
NM_001326312.2:c.2058T>C	NP_001313241.1:p.His686=
NM_001326313.2:c.1524T>C	NP_001313242.1:p.His508=
NM_001326314.2:c.1605T>C	NP_001313243.1:p.His535=
NM_001326315.2:c.2043T>C	NP_001313244.1:p.His681=
NM_207660.4:c.1677T>C	NP_997543.1:p.His559=
NM_207662.4:c.858T>C	NP_997545.2:p.His286=
NR_136936.2:n.2085T>C
NM_001326316.2:c.2043T>C	NP_001313245.1:p.His681=
NM_207661.3:c.1653T>C	NP_997544.1:p.His551=