Canonical Allele Identifier: CA390566167

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077242T>C (hg19) ; chr14:g.88610898T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610898T>C , CM000676.2:g.88610898T>C	GRCh38
NC_000014.8:g.89077242T>C , CM000676.1:g.89077242T>C	GRCh37
NC_000014.7:g.88146995T>C	NCBI36
NG_050601.1:g.52990T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2162T>C MANE Select	ENSP00000251038.5:p.Val721Ala
ENST00000649731.1:c.*1370T>C	ENSP00000497757.1:n.*1370T>C
ENST00000251038.9:c.2162T>C	ENSP00000251038.5:p.Val721Ala
ENST00000302216.12:c.1691T>C	ENSP00000307025.8:p.Val564Ala
ENST00000318308.10:c.872T>C	ENSP00000327176.6:p.Val291Ala
ENST00000336693.8:c.1667T>C	ENSP00000338002.4:p.Val556Ala
ENST00000393514.9:c.2087T>C	ENSP00000377150.5:p.Val696Ala
ENST00000406216.7:c.800T>C	ENSP00000384682.3:p.Val267Ala
ENST00000554020.5:n.1005T>C
ENST00000555755.5:c.2144T>C	ENSP00000452475.1:p.Val715Ala
ENST00000555792.1:c.407T>C	ENSP00000450823.1:p.Val136Ala
ENST00000555851.6:n.321T>C
ENST00000555900.5:c.1268T>C	ENSP00000451530.1:p.Val423Ala
ENST00000556000.5:c.1906T>C
ENST00000556945.5:c.1769T>C	ENSP00000450474.1:p.Val590Ala
ENST00000557491.1:n.1447T>C
ENST00000557607.5:c.1214T>C	ENSP00000452370.1:p.Val405Ala
NM_001160103.1:c.2159T>C	NP_001153575.1:p.Val720Ala
NM_001160104.1:c.2144T>C	NP_001153576.1:p.Val715Ala
NM_024824.4:c.2162T>C	NP_079100.2:p.Val721Ala
NM_207660.3:c.1691T>C	NP_997543.1:p.Val564Ala
NM_207661.2:c.1667T>C	NP_997544.1:p.Val556Ala
NM_207662.3:c.872T>C	NP_997545.2:p.Val291Ala
XM_005268067.3:c.2147T>C	XP_005268124.1:p.Val716Ala
XM_005268068.3:c.2087T>C	XP_005268125.1:p.Val696Ala
XM_005268069.3:c.1769T>C	XP_005268126.1:p.Val590Ala
XM_005268070.3:c.1766T>C	XP_005268127.1:p.Val589Ala
XM_005268071.3:c.1694T>C	XP_005268128.1:p.Val565Ala
XM_005268073.3:c.1268T>C	XP_005268130.1:p.Val423Ala
XM_006720257.2:c.1193T>C	XP_006720320.1:p.Val398Ala
XM_011537160.1:c.2060T>C	XP_011535462.1:p.Val687Ala
XM_011537161.1:c.2006T>C	XP_011535463.1:p.Val669Ala
NM_001326295.1:c.1769T>C	NP_001313224.1:p.Val590Ala
NM_001326296.1:c.2084T>C	NP_001313225.1:p.Val695Ala
NM_001326297.1:c.2060T>C	NP_001313226.1:p.Val687Ala
NM_001326298.1:c.1694T>C	NP_001313227.1:p.Val565Ala
NM_001326299.1:c.2069T>C	NP_001313228.1:p.Val690Ala
NM_001326300.1:c.1697T>C	NP_001313229.1:p.Val566Ala
NM_001326301.1:c.1985T>C	NP_001313230.1:p.Val662Ala
NM_001326302.1:c.1694T>C	NP_001313231.1:p.Val565Ala
NM_001326303.1:c.1589T>C	NP_001313232.1:p.Val530Ala
NM_001326304.1:c.1301T>C	NP_001313233.1:p.Val434Ala
NM_001326305.1:c.1622T>C	NP_001313234.1:p.Val541Ala
NM_001326306.1:c.1535T>C	NP_001313235.1:p.Val512Ala
NM_001326307.1:c.2087T>C	NP_001313236.1:p.Val696Ala
NM_001326308.1:c.1304T>C	NP_001313237.1:p.Val435Ala
NM_001326309.1:c.1229T>C	NP_001313238.1:p.Val410Ala
NM_001326310.1:c.2147T>C	NP_001313239.1:p.Val716Ala
NM_001326311.1:c.1226T>C	NP_001313240.1:p.Val409Ala
NM_001326312.1:c.2072T>C	NP_001313241.1:p.Val691Ala
NM_001326313.1:c.1538T>C	NP_001313242.1:p.Val513Ala
NM_001326314.1:c.1619T>C	NP_001313243.1:p.Val540Ala
NM_001326315.1:c.2057T>C	NP_001313244.1:p.Val686Ala
NM_001326316.1:c.2057T>C	NP_001313245.1:p.Val686Ala
NR_136936.1:n.2227T>C
XM_005268070.5:c.1766T>C	XP_005268127.1:p.Val589Ala
XM_005268073.4:c.1268T>C	XP_005268130.1:p.Val423Ala
XM_006720257.3:c.1193T>C	XP_006720320.1:p.Val398Ala
XM_011537161.3:c.2006T>C	XP_011535463.1:p.Val669Ala
XM_024449713.1:c.1190T>C	XP_024305481.1:p.Val397Ala
NM_024824.5:c.2162T>C MANE Select	NP_079100.2:p.Val721Ala
NM_001160103.2:c.2159T>C	NP_001153575.1:p.Val720Ala
NM_001160104.2:c.2144T>C	NP_001153576.1:p.Val715Ala
NM_001326295.2:c.1769T>C	NP_001313224.1:p.Val590Ala
NM_001326296.2:c.2084T>C	NP_001313225.1:p.Val695Ala
NM_001326297.2:c.2060T>C	NP_001313226.1:p.Val687Ala
NM_001326298.2:c.1694T>C	NP_001313227.1:p.Val565Ala
NM_001326299.2:c.2069T>C	NP_001313228.1:p.Val690Ala
NM_001326300.2:c.1697T>C	NP_001313229.1:p.Val566Ala
NM_001326301.2:c.1985T>C	NP_001313230.1:p.Val662Ala
NM_001326302.2:c.1694T>C	NP_001313231.1:p.Val565Ala
NM_001326303.2:c.1589T>C	NP_001313232.1:p.Val530Ala
NM_001326304.2:c.1301T>C	NP_001313233.1:p.Val434Ala
NM_001326305.2:c.1622T>C	NP_001313234.1:p.Val541Ala
NM_001326306.2:c.1535T>C	NP_001313235.1:p.Val512Ala
NM_001326307.2:c.2087T>C	NP_001313236.1:p.Val696Ala
NM_001326308.2:c.1304T>C	NP_001313237.1:p.Val435Ala
NM_001326309.2:c.1229T>C	NP_001313238.1:p.Val410Ala
NM_001326310.2:c.2147T>C	NP_001313239.1:p.Val716Ala
NM_001326311.2:c.1226T>C	NP_001313240.1:p.Val409Ala
NM_001326312.2:c.2072T>C	NP_001313241.1:p.Val691Ala
NM_001326313.2:c.1538T>C	NP_001313242.1:p.Val513Ala
NM_001326314.2:c.1619T>C	NP_001313243.1:p.Val540Ala
NM_001326315.2:c.2057T>C	NP_001313244.1:p.Val686Ala
NM_207660.4:c.1691T>C	NP_997543.1:p.Val564Ala
NM_207662.4:c.872T>C	NP_997545.2:p.Val291Ala
NR_136936.2:n.2099T>C
NM_001326316.2:c.2057T>C	NP_001313245.1:p.Val686Ala
NM_207661.3:c.1667T>C	NP_997544.1:p.Val556Ala