Canonical Allele Identifier: CA1328856950

Gene: ZNF142

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218650007_218650008delinsGA , CM000664.2:g.218650007_218650008delinsGA	GRCh38
NC_000002.11:g.219514730_219514731delinsGA , CM000664.1:g.219514730_219514731delinsGA	GRCh37
NC_000002.10:g.219222974_219222975delinsGA	NCBI36
NG_033099.1:g.14533_14534delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000411696.7:c.1048+351_1048+352delinsTC MANE Select	ENSP00000398798.3:n.1048+351_1048+352delinsTC
ENST00000440934.2:c.1048+351_1048+352delinsTC	ENSP00000415156.2:n.1048+351_1048+352delinsTC
ENST00000411696.6:c.448+351_448+352delinsTC	ENSP00000398798.2:n.448+351_448+352delinsTC
ENST00000433921.5:c.*273+351_*273+352delinsTC	ENSP00000405477.1:n.*273+351_*273+352delinsTC
ENST00000449707.5:c.448+351_448+352delinsTC	ENSP00000408643.1:n.448+351_448+352delinsTC
ENST00000450765.5:c.*273+351_*273+352delinsTC	ENSP00000397456.1:n.*273+351_*273+352delinsTC
NM_001105537.2:c.448+351_448+352delinsTC	NP_001099007.1:n.448+351_448+352delinsTC
NR_073599.1:n.1195+351_1195+352delinsTC
NR_073600.1:n.1028+351_1028+352delinsTC
XM_006712730.2:c.1048+351_1048+352delinsTC	XP_006712793.1:n.1048+351_1048+352delinsTC
XM_011511784.1:c.1048+351_1048+352delinsTC	XP_011510086.1:n.1048+351_1048+352delinsTC
XM_011511785.1:c.1048+351_1048+352delinsTC	XP_011510087.1:n.1048+351_1048+352delinsTC
XM_011511786.1:c.1048+351_1048+352delinsTC	XP_011510088.1:n.1048+351_1048+352delinsTC
XM_011511787.1:c.1048+351_1048+352delinsTC	XP_011510089.1:n.1048+351_1048+352delinsTC
XM_011511788.1:c.1048+351_1048+352delinsTC	XP_011510090.1:n.1048+351_1048+352delinsTC
XM_011511789.1:c.448+351_448+352delinsTC	XP_011510091.1:n.448+351_448+352delinsTC
NM_001366287.1:c.-42+351_-42+352delinsTC	NP_001353216.1:n.-42+351_-42+352delinsTC
NM_001366288.1:c.-42+351_-42+352delinsTC	NP_001353217.1:n.-42+351_-42+352delinsTC
NM_001366289.1:c.-42+351_-42+352delinsTC	NP_001353218.1:n.-42+351_-42+352delinsTC
NM_001366290.1:c.1048+351_1048+352delinsTC	NP_001353219.1:n.1048+351_1048+352delinsTC
NM_001366291.1:c.448+351_448+352delinsTC	NP_001353220.1:n.448+351_448+352delinsTC
XM_006712730.3:c.1048+351_1048+352delinsTC	XP_006712793.1:n.1048+351_1048+352delinsTC
XM_011511784.2:c.1048+351_1048+352delinsTC	XP_011510086.1:n.1048+351_1048+352delinsTC
XM_011511785.2:c.1048+351_1048+352delinsTC	XP_011510087.1:n.1048+351_1048+352delinsTC
XM_011511786.2:c.1048+351_1048+352delinsTC	XP_011510088.1:n.1048+351_1048+352delinsTC
XM_011511787.2:c.1048+351_1048+352delinsTC	XP_011510089.1:n.1048+351_1048+352delinsTC
XM_011511788.2:c.1048+351_1048+352delinsTC	XP_011510090.1:n.1048+351_1048+352delinsTC
XM_011511789.2:c.448+351_448+352delinsTC	XP_011510091.1:n.448+351_448+352delinsTC
NM_001105537.3:c.448+351_448+352delinsTC	NP_001099007.1:n.448+351_448+352delinsTC
NM_001105537.4:c.448+351_448+352delinsTC	NP_001099007.1:n.448+351_448+352delinsTC
NM_001366287.2:c.-42+351_-42+352delinsTC	NP_001353216.1:n.-42+351_-42+352delinsTC
NM_001366288.2:c.-42+351_-42+352delinsTC	NP_001353217.1:n.-42+351_-42+352delinsTC
NM_001366289.2:c.-42+351_-42+352delinsTC	NP_001353218.1:n.-42+351_-42+352delinsTC
NM_001366290.3:c.1048+351_1048+352delinsTC	NP_001353219.1:n.1048+351_1048+352delinsTC
NM_001366291.2:c.448+351_448+352delinsTC	NP_001353220.1:n.448+351_448+352delinsTC
NM_001379659.1:c.1048+351_1048+352delinsTC MANE Select	NP_001366588.1:n.1048+351_1048+352delinsTC
NM_001379660.1:c.1048+351_1048+352delinsTC	NP_001366589.1:n.1048+351_1048+352delinsTC
NM_001379661.1:c.1048+351_1048+352delinsTC	NP_001366590.1:n.1048+351_1048+352delinsTC
NM_001379662.1:c.448+351_448+352delinsTC	NP_001366591.1:n.448+351_448+352delinsTC