Canonical Allele Identifier: CA390565788

Gene: ZC3H14

Linked Data

• gnomAD v4: 14-88610858-A-G
• MyVariant Identifiers: chr14:g.89077202A>G (hg19) ; chr14:g.88610858A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88610858A>G , CM000676.2:g.88610858A>G	GRCh38
NC_000014.8:g.89077202A>G , CM000676.1:g.89077202A>G	GRCh37
NC_000014.7:g.88146955A>G	NCBI36
NG_050601.1:g.52950A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251038.10:c.2122A>G MANE Select	ENSP00000251038.5:p.Thr708Ala
ENST00000649731.1:c.*1330A>G	ENSP00000497757.1:n.*1330A>G
ENST00000251038.9:c.2122A>G	ENSP00000251038.5:p.Thr708Ala
ENST00000302216.12:c.1651A>G	ENSP00000307025.8:p.Thr551Ala
ENST00000318308.10:c.832A>G	ENSP00000327176.6:p.Thr278Ala
ENST00000336693.8:c.1627A>G	ENSP00000338002.4:p.Thr543Ala
ENST00000393514.9:c.2047A>G	ENSP00000377150.5:p.Thr683Ala
ENST00000406216.7:c.760A>G	ENSP00000384682.3:p.Thr254Ala
ENST00000554020.5:n.965A>G
ENST00000555755.5:c.2104A>G	ENSP00000452475.1:p.Thr702Ala
ENST00000555792.1:c.367A>G	ENSP00000450823.1:p.Thr123Ala
ENST00000555851.6:n.281A>G
ENST00000555900.5:c.1228A>G	ENSP00000451530.1:p.Thr410Ala
ENST00000556000.5:c.1866A>G
ENST00000556945.5:c.1729A>G	ENSP00000450474.1:p.Thr577Ala
ENST00000557491.1:n.1407A>G
ENST00000557607.5:c.1174A>G	ENSP00000452370.1:p.Thr392Ala
NM_001160103.1:c.2119A>G	NP_001153575.1:p.Thr707Ala
NM_001160104.1:c.2104A>G	NP_001153576.1:p.Thr702Ala
NM_024824.4:c.2122A>G	NP_079100.2:p.Thr708Ala
NM_207660.3:c.1651A>G	NP_997543.1:p.Thr551Ala
NM_207661.2:c.1627A>G	NP_997544.1:p.Thr543Ala
NM_207662.3:c.832A>G	NP_997545.2:p.Thr278Ala
XM_005268067.3:c.2107A>G	XP_005268124.1:p.Thr703Ala
XM_005268068.3:c.2047A>G	XP_005268125.1:p.Thr683Ala
XM_005268069.3:c.1729A>G	XP_005268126.1:p.Thr577Ala
XM_005268070.3:c.1726A>G	XP_005268127.1:p.Thr576Ala
XM_005268071.3:c.1654A>G	XP_005268128.1:p.Thr552Ala
XM_005268073.3:c.1228A>G	XP_005268130.1:p.Thr410Ala
XM_006720257.2:c.1153A>G	XP_006720320.1:p.Thr385Ala
XM_011537160.1:c.2020A>G	XP_011535462.1:p.Thr674Ala
XM_011537161.1:c.1966A>G	XP_011535463.1:p.Thr656Ala
NM_001326295.1:c.1729A>G	NP_001313224.1:p.Thr577Ala
NM_001326296.1:c.2044A>G	NP_001313225.1:p.Thr682Ala
NM_001326297.1:c.2020A>G	NP_001313226.1:p.Thr674Ala
NM_001326298.1:c.1654A>G	NP_001313227.1:p.Thr552Ala
NM_001326299.1:c.2029A>G	NP_001313228.1:p.Thr677Ala
NM_001326300.1:c.1657A>G	NP_001313229.1:p.Thr553Ala
NM_001326301.1:c.1945A>G	NP_001313230.1:p.Thr649Ala
NM_001326302.1:c.1654A>G	NP_001313231.1:p.Thr552Ala
NM_001326303.1:c.1549A>G	NP_001313232.1:p.Thr517Ala
NM_001326304.1:c.1261A>G	NP_001313233.1:p.Thr421Ala
NM_001326305.1:c.1582A>G	NP_001313234.1:p.Thr528Ala
NM_001326306.1:c.1495A>G	NP_001313235.1:p.Thr499Ala
NM_001326307.1:c.2047A>G	NP_001313236.1:p.Thr683Ala
NM_001326308.1:c.1264A>G	NP_001313237.1:p.Thr422Ala
NM_001326309.1:c.1189A>G	NP_001313238.1:p.Thr397Ala
NM_001326310.1:c.2107A>G	NP_001313239.1:p.Thr703Ala
NM_001326311.1:c.1186A>G	NP_001313240.1:p.Thr396Ala
NM_001326312.1:c.2032A>G	NP_001313241.1:p.Thr678Ala
NM_001326313.1:c.1498A>G	NP_001313242.1:p.Thr500Ala
NM_001326314.1:c.1579A>G	NP_001313243.1:p.Thr527Ala
NM_001326315.1:c.2017A>G	NP_001313244.1:p.Thr673Ala
NM_001326316.1:c.2017A>G	NP_001313245.1:p.Thr673Ala
NR_136936.1:n.2187A>G
XM_005268070.5:c.1726A>G	XP_005268127.1:p.Thr576Ala
XM_005268073.4:c.1228A>G	XP_005268130.1:p.Thr410Ala
XM_006720257.3:c.1153A>G	XP_006720320.1:p.Thr385Ala
XM_011537161.3:c.1966A>G	XP_011535463.1:p.Thr656Ala
XM_024449713.1:c.1150A>G	XP_024305481.1:p.Thr384Ala
NM_024824.5:c.2122A>G MANE Select	NP_079100.2:p.Thr708Ala
NM_001160103.2:c.2119A>G	NP_001153575.1:p.Thr707Ala
NM_001160104.2:c.2104A>G	NP_001153576.1:p.Thr702Ala
NM_001326295.2:c.1729A>G	NP_001313224.1:p.Thr577Ala
NM_001326296.2:c.2044A>G	NP_001313225.1:p.Thr682Ala
NM_001326297.2:c.2020A>G	NP_001313226.1:p.Thr674Ala
NM_001326298.2:c.1654A>G	NP_001313227.1:p.Thr552Ala
NM_001326299.2:c.2029A>G	NP_001313228.1:p.Thr677Ala
NM_001326300.2:c.1657A>G	NP_001313229.1:p.Thr553Ala
NM_001326301.2:c.1945A>G	NP_001313230.1:p.Thr649Ala
NM_001326302.2:c.1654A>G	NP_001313231.1:p.Thr552Ala
NM_001326303.2:c.1549A>G	NP_001313232.1:p.Thr517Ala
NM_001326304.2:c.1261A>G	NP_001313233.1:p.Thr421Ala
NM_001326305.2:c.1582A>G	NP_001313234.1:p.Thr528Ala
NM_001326306.2:c.1495A>G	NP_001313235.1:p.Thr499Ala
NM_001326307.2:c.2047A>G	NP_001313236.1:p.Thr683Ala
NM_001326308.2:c.1264A>G	NP_001313237.1:p.Thr422Ala
NM_001326309.2:c.1189A>G	NP_001313238.1:p.Thr397Ala
NM_001326310.2:c.2107A>G	NP_001313239.1:p.Thr703Ala
NM_001326311.2:c.1186A>G	NP_001313240.1:p.Thr396Ala
NM_001326312.2:c.2032A>G	NP_001313241.1:p.Thr678Ala
NM_001326313.2:c.1498A>G	NP_001313242.1:p.Thr500Ala
NM_001326314.2:c.1579A>G	NP_001313243.1:p.Thr527Ala
NM_001326315.2:c.2017A>G	NP_001313244.1:p.Thr673Ala
NM_207660.4:c.1651A>G	NP_997543.1:p.Thr551Ala
NM_207662.4:c.832A>G	NP_997545.2:p.Thr278Ala
NR_136936.2:n.2059A>G
NM_001326316.2:c.2017A>G	NP_001313245.1:p.Thr673Ala
NM_207661.3:c.1627A>G	NP_997544.1:p.Thr543Ala