Canonical Allele Identifier: CA390565935

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077215G>C (hg19) ; chr14:g.88610871G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610871G>C , CM000676.2:g.88610871G>C	GRCh38
NC_000014.8:g.89077215G>C , CM000676.1:g.89077215G>C	GRCh37
NC_000014.7:g.88146968G>C	NCBI36
NG_050601.1:g.52963G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2135G>C MANE Select	ENSP00000251038.5:p.Cys712Ser
ENST00000649731.1:c.*1343G>C	ENSP00000497757.1:n.*1343G>C
ENST00000251038.9:c.2135G>C	ENSP00000251038.5:p.Cys712Ser
ENST00000302216.12:c.1664G>C	ENSP00000307025.8:p.Cys555Ser
ENST00000318308.10:c.845G>C	ENSP00000327176.6:p.Cys282Ser
ENST00000336693.8:c.1640G>C	ENSP00000338002.4:p.Cys547Ser
ENST00000393514.9:c.2060G>C	ENSP00000377150.5:p.Cys687Ser
ENST00000406216.7:c.773G>C	ENSP00000384682.3:p.Cys258Ser
ENST00000554020.5:n.978G>C
ENST00000555755.5:c.2117G>C	ENSP00000452475.1:p.Cys706Ser
ENST00000555792.1:c.380G>C	ENSP00000450823.1:p.Cys127Ser
ENST00000555851.6:n.294G>C
ENST00000555900.5:c.1241G>C	ENSP00000451530.1:p.Cys414Ser
ENST00000556000.5:c.1879G>C
ENST00000556945.5:c.1742G>C	ENSP00000450474.1:p.Cys581Ser
ENST00000557491.1:n.1420G>C
ENST00000557607.5:c.1187G>C	ENSP00000452370.1:p.Cys396Ser
NM_001160103.1:c.2132G>C	NP_001153575.1:p.Cys711Ser
NM_001160104.1:c.2117G>C	NP_001153576.1:p.Cys706Ser
NM_024824.4:c.2135G>C	NP_079100.2:p.Cys712Ser
NM_207660.3:c.1664G>C	NP_997543.1:p.Cys555Ser
NM_207661.2:c.1640G>C	NP_997544.1:p.Cys547Ser
NM_207662.3:c.845G>C	NP_997545.2:p.Cys282Ser
XM_005268067.3:c.2120G>C	XP_005268124.1:p.Cys707Ser
XM_005268068.3:c.2060G>C	XP_005268125.1:p.Cys687Ser
XM_005268069.3:c.1742G>C	XP_005268126.1:p.Cys581Ser
XM_005268070.3:c.1739G>C	XP_005268127.1:p.Cys580Ser
XM_005268071.3:c.1667G>C	XP_005268128.1:p.Cys556Ser
XM_005268073.3:c.1241G>C	XP_005268130.1:p.Cys414Ser
XM_006720257.2:c.1166G>C	XP_006720320.1:p.Cys389Ser
XM_011537160.1:c.2033G>C	XP_011535462.1:p.Cys678Ser
XM_011537161.1:c.1979G>C	XP_011535463.1:p.Cys660Ser
NM_001326295.1:c.1742G>C	NP_001313224.1:p.Cys581Ser
NM_001326296.1:c.2057G>C	NP_001313225.1:p.Cys686Ser
NM_001326297.1:c.2033G>C	NP_001313226.1:p.Cys678Ser
NM_001326298.1:c.1667G>C	NP_001313227.1:p.Cys556Ser
NM_001326299.1:c.2042G>C	NP_001313228.1:p.Cys681Ser
NM_001326300.1:c.1670G>C	NP_001313229.1:p.Cys557Ser
NM_001326301.1:c.1958G>C	NP_001313230.1:p.Cys653Ser
NM_001326302.1:c.1667G>C	NP_001313231.1:p.Cys556Ser
NM_001326303.1:c.1562G>C	NP_001313232.1:p.Cys521Ser
NM_001326304.1:c.1274G>C	NP_001313233.1:p.Cys425Ser
NM_001326305.1:c.1595G>C	NP_001313234.1:p.Cys532Ser
NM_001326306.1:c.1508G>C	NP_001313235.1:p.Cys503Ser
NM_001326307.1:c.2060G>C	NP_001313236.1:p.Cys687Ser
NM_001326308.1:c.1277G>C	NP_001313237.1:p.Cys426Ser
NM_001326309.1:c.1202G>C	NP_001313238.1:p.Cys401Ser
NM_001326310.1:c.2120G>C	NP_001313239.1:p.Cys707Ser
NM_001326311.1:c.1199G>C	NP_001313240.1:p.Cys400Ser
NM_001326312.1:c.2045G>C	NP_001313241.1:p.Cys682Ser
NM_001326313.1:c.1511G>C	NP_001313242.1:p.Cys504Ser
NM_001326314.1:c.1592G>C	NP_001313243.1:p.Cys531Ser
NM_001326315.1:c.2030G>C	NP_001313244.1:p.Cys677Ser
NM_001326316.1:c.2030G>C	NP_001313245.1:p.Cys677Ser
NR_136936.1:n.2200G>C
XM_005268070.5:c.1739G>C	XP_005268127.1:p.Cys580Ser
XM_005268073.4:c.1241G>C	XP_005268130.1:p.Cys414Ser
XM_006720257.3:c.1166G>C	XP_006720320.1:p.Cys389Ser
XM_011537161.3:c.1979G>C	XP_011535463.1:p.Cys660Ser
XM_024449713.1:c.1163G>C	XP_024305481.1:p.Cys388Ser
NM_024824.5:c.2135G>C MANE Select	NP_079100.2:p.Cys712Ser
NM_001160103.2:c.2132G>C	NP_001153575.1:p.Cys711Ser
NM_001160104.2:c.2117G>C	NP_001153576.1:p.Cys706Ser
NM_001326295.2:c.1742G>C	NP_001313224.1:p.Cys581Ser
NM_001326296.2:c.2057G>C	NP_001313225.1:p.Cys686Ser
NM_001326297.2:c.2033G>C	NP_001313226.1:p.Cys678Ser
NM_001326298.2:c.1667G>C	NP_001313227.1:p.Cys556Ser
NM_001326299.2:c.2042G>C	NP_001313228.1:p.Cys681Ser
NM_001326300.2:c.1670G>C	NP_001313229.1:p.Cys557Ser
NM_001326301.2:c.1958G>C	NP_001313230.1:p.Cys653Ser
NM_001326302.2:c.1667G>C	NP_001313231.1:p.Cys556Ser
NM_001326303.2:c.1562G>C	NP_001313232.1:p.Cys521Ser
NM_001326304.2:c.1274G>C	NP_001313233.1:p.Cys425Ser
NM_001326305.2:c.1595G>C	NP_001313234.1:p.Cys532Ser
NM_001326306.2:c.1508G>C	NP_001313235.1:p.Cys503Ser
NM_001326307.2:c.2060G>C	NP_001313236.1:p.Cys687Ser
NM_001326308.2:c.1277G>C	NP_001313237.1:p.Cys426Ser
NM_001326309.2:c.1202G>C	NP_001313238.1:p.Cys401Ser
NM_001326310.2:c.2120G>C	NP_001313239.1:p.Cys707Ser
NM_001326311.2:c.1199G>C	NP_001313240.1:p.Cys400Ser
NM_001326312.2:c.2045G>C	NP_001313241.1:p.Cys682Ser
NM_001326313.2:c.1511G>C	NP_001313242.1:p.Cys504Ser
NM_001326314.2:c.1592G>C	NP_001313243.1:p.Cys531Ser
NM_001326315.2:c.2030G>C	NP_001313244.1:p.Cys677Ser
NM_207660.4:c.1664G>C	NP_997543.1:p.Cys555Ser
NM_207662.4:c.845G>C	NP_997545.2:p.Cys282Ser
NR_136936.2:n.2072G>C
NM_001326316.2:c.2030G>C	NP_001313245.1:p.Cys677Ser
NM_207661.3:c.1640G>C	NP_997544.1:p.Cys547Ser