Canonical Allele Identifier: CA390566064

Gene: ZC3H14

Linked Data

• MyVariant Identifiers: chr14:g.89077229C>A (hg19) ; chr14:g.88610885C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610885C>A , CM000676.2:g.88610885C>A	GRCh38
NC_000014.8:g.89077229C>A , CM000676.1:g.89077229C>A	GRCh37
NC_000014.7:g.88146982C>A	NCBI36
NG_050601.1:g.52977C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2149C>A MANE Select	ENSP00000251038.5:p.Pro717Thr
ENST00000649731.1:c.*1357C>A	ENSP00000497757.1:n.*1357C>A
ENST00000251038.9:c.2149C>A	ENSP00000251038.5:p.Pro717Thr
ENST00000302216.12:c.1678C>A	ENSP00000307025.8:p.Pro560Thr
ENST00000318308.10:c.859C>A	ENSP00000327176.6:p.Pro287Thr
ENST00000336693.8:c.1654C>A	ENSP00000338002.4:p.Pro552Thr
ENST00000393514.9:c.2074C>A	ENSP00000377150.5:p.Pro692Thr
ENST00000406216.7:c.787C>A	ENSP00000384682.3:p.Pro263Thr
ENST00000554020.5:n.992C>A
ENST00000555755.5:c.2131C>A	ENSP00000452475.1:p.Pro711Thr
ENST00000555792.1:c.394C>A	ENSP00000450823.1:p.Pro132Thr
ENST00000555851.6:n.308C>A
ENST00000555900.5:c.1255C>A	ENSP00000451530.1:p.Pro419Thr
ENST00000556000.5:c.1893C>A
ENST00000556945.5:c.1756C>A	ENSP00000450474.1:p.Pro586Thr
ENST00000557491.1:n.1434C>A
ENST00000557607.5:c.1201C>A	ENSP00000452370.1:p.Pro401Thr
NM_001160103.1:c.2146C>A	NP_001153575.1:p.Pro716Thr
NM_001160104.1:c.2131C>A	NP_001153576.1:p.Pro711Thr
NM_024824.4:c.2149C>A	NP_079100.2:p.Pro717Thr
NM_207660.3:c.1678C>A	NP_997543.1:p.Pro560Thr
NM_207661.2:c.1654C>A	NP_997544.1:p.Pro552Thr
NM_207662.3:c.859C>A	NP_997545.2:p.Pro287Thr
XM_005268067.3:c.2134C>A	XP_005268124.1:p.Pro712Thr
XM_005268068.3:c.2074C>A	XP_005268125.1:p.Pro692Thr
XM_005268069.3:c.1756C>A	XP_005268126.1:p.Pro586Thr
XM_005268070.3:c.1753C>A	XP_005268127.1:p.Pro585Thr
XM_005268071.3:c.1681C>A	XP_005268128.1:p.Pro561Thr
XM_005268073.3:c.1255C>A	XP_005268130.1:p.Pro419Thr
XM_006720257.2:c.1180C>A	XP_006720320.1:p.Pro394Thr
XM_011537160.1:c.2047C>A	XP_011535462.1:p.Pro683Thr
XM_011537161.1:c.1993C>A	XP_011535463.1:p.Pro665Thr
NM_001326295.1:c.1756C>A	NP_001313224.1:p.Pro586Thr
NM_001326296.1:c.2071C>A	NP_001313225.1:p.Pro691Thr
NM_001326297.1:c.2047C>A	NP_001313226.1:p.Pro683Thr
NM_001326298.1:c.1681C>A	NP_001313227.1:p.Pro561Thr
NM_001326299.1:c.2056C>A	NP_001313228.1:p.Pro686Thr
NM_001326300.1:c.1684C>A	NP_001313229.1:p.Pro562Thr
NM_001326301.1:c.1972C>A	NP_001313230.1:p.Pro658Thr
NM_001326302.1:c.1681C>A	NP_001313231.1:p.Pro561Thr
NM_001326303.1:c.1576C>A	NP_001313232.1:p.Pro526Thr
NM_001326304.1:c.1288C>A	NP_001313233.1:p.Pro430Thr
NM_001326305.1:c.1609C>A	NP_001313234.1:p.Pro537Thr
NM_001326306.1:c.1522C>A	NP_001313235.1:p.Pro508Thr
NM_001326307.1:c.2074C>A	NP_001313236.1:p.Pro692Thr
NM_001326308.1:c.1291C>A	NP_001313237.1:p.Pro431Thr
NM_001326309.1:c.1216C>A	NP_001313238.1:p.Pro406Thr
NM_001326310.1:c.2134C>A	NP_001313239.1:p.Pro712Thr
NM_001326311.1:c.1213C>A	NP_001313240.1:p.Pro405Thr
NM_001326312.1:c.2059C>A	NP_001313241.1:p.Pro687Thr
NM_001326313.1:c.1525C>A	NP_001313242.1:p.Pro509Thr
NM_001326314.1:c.1606C>A	NP_001313243.1:p.Pro536Thr
NM_001326315.1:c.2044C>A	NP_001313244.1:p.Pro682Thr
NM_001326316.1:c.2044C>A	NP_001313245.1:p.Pro682Thr
NR_136936.1:n.2214C>A
XM_005268070.5:c.1753C>A	XP_005268127.1:p.Pro585Thr
XM_005268073.4:c.1255C>A	XP_005268130.1:p.Pro419Thr
XM_006720257.3:c.1180C>A	XP_006720320.1:p.Pro394Thr
XM_011537161.3:c.1993C>A	XP_011535463.1:p.Pro665Thr
XM_024449713.1:c.1177C>A	XP_024305481.1:p.Pro393Thr
NM_024824.5:c.2149C>A MANE Select	NP_079100.2:p.Pro717Thr
NM_001160103.2:c.2146C>A	NP_001153575.1:p.Pro716Thr
NM_001160104.2:c.2131C>A	NP_001153576.1:p.Pro711Thr
NM_001326295.2:c.1756C>A	NP_001313224.1:p.Pro586Thr
NM_001326296.2:c.2071C>A	NP_001313225.1:p.Pro691Thr
NM_001326297.2:c.2047C>A	NP_001313226.1:p.Pro683Thr
NM_001326298.2:c.1681C>A	NP_001313227.1:p.Pro561Thr
NM_001326299.2:c.2056C>A	NP_001313228.1:p.Pro686Thr
NM_001326300.2:c.1684C>A	NP_001313229.1:p.Pro562Thr
NM_001326301.2:c.1972C>A	NP_001313230.1:p.Pro658Thr
NM_001326302.2:c.1681C>A	NP_001313231.1:p.Pro561Thr
NM_001326303.2:c.1576C>A	NP_001313232.1:p.Pro526Thr
NM_001326304.2:c.1288C>A	NP_001313233.1:p.Pro430Thr
NM_001326305.2:c.1609C>A	NP_001313234.1:p.Pro537Thr
NM_001326306.2:c.1522C>A	NP_001313235.1:p.Pro508Thr
NM_001326307.2:c.2074C>A	NP_001313236.1:p.Pro692Thr
NM_001326308.2:c.1291C>A	NP_001313237.1:p.Pro431Thr
NM_001326309.2:c.1216C>A	NP_001313238.1:p.Pro406Thr
NM_001326310.2:c.2134C>A	NP_001313239.1:p.Pro712Thr
NM_001326311.2:c.1213C>A	NP_001313240.1:p.Pro405Thr
NM_001326312.2:c.2059C>A	NP_001313241.1:p.Pro687Thr
NM_001326313.2:c.1525C>A	NP_001313242.1:p.Pro509Thr
NM_001326314.2:c.1606C>A	NP_001313243.1:p.Pro536Thr
NM_001326315.2:c.2044C>A	NP_001313244.1:p.Pro682Thr
NM_207660.4:c.1678C>A	NP_997543.1:p.Pro560Thr
NM_207662.4:c.859C>A	NP_997545.2:p.Pro287Thr
NR_136936.2:n.2086C>A
NM_001326316.2:c.2044C>A	NP_001313245.1:p.Pro682Thr
NM_207661.3:c.1654C>A	NP_997544.1:p.Pro552Thr