Canonical Allele Identifier: CA390565827

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077208C>G (hg19) ; chr14:g.88610864C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610864C>G , CM000676.2:g.88610864C>G	GRCh38
NC_000014.8:g.89077208C>G , CM000676.1:g.89077208C>G	GRCh37
NC_000014.7:g.88146961C>G	NCBI36
NG_050601.1:g.52956C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2128C>G MANE Select	ENSP00000251038.5:p.Pro710Ala
ENST00000649731.1:c.*1336C>G	ENSP00000497757.1:n.*1336C>G
ENST00000251038.9:c.2128C>G	ENSP00000251038.5:p.Pro710Ala
ENST00000302216.12:c.1657C>G	ENSP00000307025.8:p.Pro553Ala
ENST00000318308.10:c.838C>G	ENSP00000327176.6:p.Pro280Ala
ENST00000336693.8:c.1633C>G	ENSP00000338002.4:p.Pro545Ala
ENST00000393514.9:c.2053C>G	ENSP00000377150.5:p.Pro685Ala
ENST00000406216.7:c.766C>G	ENSP00000384682.3:p.Pro256Ala
ENST00000554020.5:n.971C>G
ENST00000555755.5:c.2110C>G	ENSP00000452475.1:p.Pro704Ala
ENST00000555792.1:c.373C>G	ENSP00000450823.1:p.Pro125Ala
ENST00000555851.6:n.287C>G
ENST00000555900.5:c.1234C>G	ENSP00000451530.1:p.Pro412Ala
ENST00000556000.5:c.1872C>G
ENST00000556945.5:c.1735C>G	ENSP00000450474.1:p.Pro579Ala
ENST00000557491.1:n.1413C>G
ENST00000557607.5:c.1180C>G	ENSP00000452370.1:p.Pro394Ala
NM_001160103.1:c.2125C>G	NP_001153575.1:p.Pro709Ala
NM_001160104.1:c.2110C>G	NP_001153576.1:p.Pro704Ala
NM_024824.4:c.2128C>G	NP_079100.2:p.Pro710Ala
NM_207660.3:c.1657C>G	NP_997543.1:p.Pro553Ala
NM_207661.2:c.1633C>G	NP_997544.1:p.Pro545Ala
NM_207662.3:c.838C>G	NP_997545.2:p.Pro280Ala
XM_005268067.3:c.2113C>G	XP_005268124.1:p.Pro705Ala
XM_005268068.3:c.2053C>G	XP_005268125.1:p.Pro685Ala
XM_005268069.3:c.1735C>G	XP_005268126.1:p.Pro579Ala
XM_005268070.3:c.1732C>G	XP_005268127.1:p.Pro578Ala
XM_005268071.3:c.1660C>G	XP_005268128.1:p.Pro554Ala
XM_005268073.3:c.1234C>G	XP_005268130.1:p.Pro412Ala
XM_006720257.2:c.1159C>G	XP_006720320.1:p.Pro387Ala
XM_011537160.1:c.2026C>G	XP_011535462.1:p.Pro676Ala
XM_011537161.1:c.1972C>G	XP_011535463.1:p.Pro658Ala
NM_001326295.1:c.1735C>G	NP_001313224.1:p.Pro579Ala
NM_001326296.1:c.2050C>G	NP_001313225.1:p.Pro684Ala
NM_001326297.1:c.2026C>G	NP_001313226.1:p.Pro676Ala
NM_001326298.1:c.1660C>G	NP_001313227.1:p.Pro554Ala
NM_001326299.1:c.2035C>G	NP_001313228.1:p.Pro679Ala
NM_001326300.1:c.1663C>G	NP_001313229.1:p.Pro555Ala
NM_001326301.1:c.1951C>G	NP_001313230.1:p.Pro651Ala
NM_001326302.1:c.1660C>G	NP_001313231.1:p.Pro554Ala
NM_001326303.1:c.1555C>G	NP_001313232.1:p.Pro519Ala
NM_001326304.1:c.1267C>G	NP_001313233.1:p.Pro423Ala
NM_001326305.1:c.1588C>G	NP_001313234.1:p.Pro530Ala
NM_001326306.1:c.1501C>G	NP_001313235.1:p.Pro501Ala
NM_001326307.1:c.2053C>G	NP_001313236.1:p.Pro685Ala
NM_001326308.1:c.1270C>G	NP_001313237.1:p.Pro424Ala
NM_001326309.1:c.1195C>G	NP_001313238.1:p.Pro399Ala
NM_001326310.1:c.2113C>G	NP_001313239.1:p.Pro705Ala
NM_001326311.1:c.1192C>G	NP_001313240.1:p.Pro398Ala
NM_001326312.1:c.2038C>G	NP_001313241.1:p.Pro680Ala
NM_001326313.1:c.1504C>G	NP_001313242.1:p.Pro502Ala
NM_001326314.1:c.1585C>G	NP_001313243.1:p.Pro529Ala
NM_001326315.1:c.2023C>G	NP_001313244.1:p.Pro675Ala
NM_001326316.1:c.2023C>G	NP_001313245.1:p.Pro675Ala
NR_136936.1:n.2193C>G
XM_005268070.5:c.1732C>G	XP_005268127.1:p.Pro578Ala
XM_005268073.4:c.1234C>G	XP_005268130.1:p.Pro412Ala
XM_006720257.3:c.1159C>G	XP_006720320.1:p.Pro387Ala
XM_011537161.3:c.1972C>G	XP_011535463.1:p.Pro658Ala
XM_024449713.1:c.1156C>G	XP_024305481.1:p.Pro386Ala
NM_024824.5:c.2128C>G MANE Select	NP_079100.2:p.Pro710Ala
NM_001160103.2:c.2125C>G	NP_001153575.1:p.Pro709Ala
NM_001160104.2:c.2110C>G	NP_001153576.1:p.Pro704Ala
NM_001326295.2:c.1735C>G	NP_001313224.1:p.Pro579Ala
NM_001326296.2:c.2050C>G	NP_001313225.1:p.Pro684Ala
NM_001326297.2:c.2026C>G	NP_001313226.1:p.Pro676Ala
NM_001326298.2:c.1660C>G	NP_001313227.1:p.Pro554Ala
NM_001326299.2:c.2035C>G	NP_001313228.1:p.Pro679Ala
NM_001326300.2:c.1663C>G	NP_001313229.1:p.Pro555Ala
NM_001326301.2:c.1951C>G	NP_001313230.1:p.Pro651Ala
NM_001326302.2:c.1660C>G	NP_001313231.1:p.Pro554Ala
NM_001326303.2:c.1555C>G	NP_001313232.1:p.Pro519Ala
NM_001326304.2:c.1267C>G	NP_001313233.1:p.Pro423Ala
NM_001326305.2:c.1588C>G	NP_001313234.1:p.Pro530Ala
NM_001326306.2:c.1501C>G	NP_001313235.1:p.Pro501Ala
NM_001326307.2:c.2053C>G	NP_001313236.1:p.Pro685Ala
NM_001326308.2:c.1270C>G	NP_001313237.1:p.Pro424Ala
NM_001326309.2:c.1195C>G	NP_001313238.1:p.Pro399Ala
NM_001326310.2:c.2113C>G	NP_001313239.1:p.Pro705Ala
NM_001326311.2:c.1192C>G	NP_001313240.1:p.Pro398Ala
NM_001326312.2:c.2038C>G	NP_001313241.1:p.Pro680Ala
NM_001326313.2:c.1504C>G	NP_001313242.1:p.Pro502Ala
NM_001326314.2:c.1585C>G	NP_001313243.1:p.Pro529Ala
NM_001326315.2:c.2023C>G	NP_001313244.1:p.Pro675Ala
NM_207660.4:c.1657C>G	NP_997543.1:p.Pro553Ala
NM_207662.4:c.838C>G	NP_997545.2:p.Pro280Ala
NR_136936.2:n.2065C>G
NM_001326316.2:c.2023C>G	NP_001313245.1:p.Pro675Ala
NM_207661.3:c.1633C>G	NP_997544.1:p.Pro545Ala