Canonical Allele Identifier: CA2108604

Gene: ZNF142

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218640760G>A , CM000664.2:g.218640760G>A	GRCh38
NC_000002.11:g.219505483G>A , CM000664.1:g.219505483G>A	GRCh37
NC_000002.10:g.219213727G>A	NCBI36
NG_033099.1:g.23781C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001379659.1:c.5098C>T MANE Select	NP_001366588.1:p.Arg1700Trp
ENST00000411696.7:c.5098C>T MANE Select	ENSP00000398798.3:p.Arg1700Trp
NM_001105537.2:c.4498C>T	NP_001099007.1:p.Arg1500Trp
NM_001105537.3:c.4498C>T	NP_001099007.1:p.Arg1500Trp
NM_001105537.4:c.4498C>T	NP_001099007.1:p.Arg1500Trp
NM_001366287.1:c.4009C>T	NP_001353216.1:p.Arg1337Trp
NM_001366287.2:c.4009C>T	NP_001353216.1:p.Arg1337Trp
NM_001366288.1:c.4009C>T	NP_001353217.1:p.Arg1337Trp
NM_001366288.2:c.4009C>T	NP_001353217.1:p.Arg1337Trp
NM_001366289.1:c.4009C>T	NP_001353218.1:p.Arg1337Trp
NM_001366289.2:c.4009C>T	NP_001353218.1:p.Arg1337Trp
NM_001366290.1:c.5098C>T	NP_001353219.1:p.Arg1700Trp
NM_001366290.3:c.5098C>T	NP_001353219.1:p.Arg1700Trp
NM_001366291.1:c.4498C>T	NP_001353220.1:p.Arg1500Trp
NM_001366291.2:c.4498C>T	NP_001353220.1:p.Arg1500Trp
NM_001379660.1:c.5098C>T	NP_001366589.1:p.Arg1700Trp
NM_001379661.1:c.5098C>T	NP_001366590.1:p.Arg1700Trp
NM_001379662.1:c.4498C>T	NP_001366591.1:p.Arg1500Trp
NR_073599.1:n.5245C>T
NR_073600.1:n.5078C>T
ENST00000411696.6:c.4498C>T	ENSP00000398798.2:p.Arg1500Trp
ENST00000433921.5:c.*4323C>T	ENSP00000405477.1:n.*4323C>T
ENST00000449707.5:c.4498C>T	ENSP00000408643.1:p.Arg1500Trp
ENST00000450765.5:c.*4323C>T	ENSP00000397456.1:n.*4323C>T
XM_006712730.2:c.5098C>T	XP_006712793.1:p.Arg1700Trp
XM_006712730.3:c.5098C>T	XP_006712793.1:p.Arg1700Trp
XM_011511784.1:c.5098C>T	XP_011510086.1:p.Arg1700Trp
XM_011511784.2:c.5098C>T	XP_011510086.1:p.Arg1700Trp
XM_011511785.1:c.5098C>T	XP_011510087.1:p.Arg1700Trp
XM_011511785.2:c.5098C>T	XP_011510087.1:p.Arg1700Trp
XM_011511786.1:c.5098C>T	XP_011510088.1:p.Arg1700Trp
XM_011511786.2:c.5098C>T	XP_011510088.1:p.Arg1700Trp
XM_011511787.1:c.5098C>T	XP_011510089.1:p.Arg1700Trp
XM_011511787.2:c.5098C>T	XP_011510089.1:p.Arg1700Trp
XM_011511788.1:c.5098C>T	XP_011510090.1:p.Arg1700Trp
XM_011511788.2:c.5098C>T	XP_011510090.1:p.Arg1700Trp
XM_011511789.1:c.4498C>T	XP_011510091.1:p.Arg1500Trp
XM_011511789.2:c.4498C>T	XP_011510091.1:p.Arg1500Trp