Canonical Allele Identifier: CA206300015

Gene: ZNF239

Linked Data

• dbSNP Id: rs775117602
• MyVariant Identifiers: chr10:g.44068667_44068671del (hg19) ; chr10:g.43573219_43573223del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43573225_43573229del , CM000672.2:g.43573225_43573229del	GRCh38
NC_000010.10:g.44068673_44068677del , CM000672.1:g.44068673_44068677del	GRCh37
NC_000010.9:g.43388679_43388683del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374446.7:c.-216+414_-216+418del MANE Select	ENSP00000363569.1:n.-216+414_-216+418del
ENST00000374446.6:c.-216+414_-216+418del	ENSP00000363569.1:n.-216+414_-216+418del
ENST00000426961.1:c.-216+1317_-216+1321del	ENSP00000398202.1:n.-216+1317_-216+1321del
ENST00000491188.1:n.58+1317_58+1321del
ENST00000535642.5:c.-93+1317_-93+1321del	ENSP00000443907.1:n.-93+1317_-93+1321del
NM_001099282.1:c.-216+414_-216+418del	NP_001092752.1:n.-216+414_-216+418del
NM_001099283.1:c.-93+1317_-93+1321del	NP_001092753.1:n.-93+1317_-93+1321del
NM_001099284.1:c.-216+1317_-216+1321del	NP_001092754.1:n.-216+1317_-216+1321del
XM_005271828.1:c.-216+414_-216+418del	XP_005271885.1:n.-216+414_-216+418del
XM_005271829.1:c.-216+1248_-216+1252del	XP_005271886.1:n.-216+1248_-216+1252del
XM_005271831.1:c.-93+1248_-93+1252del	XP_005271888.1:n.-93+1248_-93+1252del
XM_006718002.1:c.-93+414_-93+418del	XP_006718065.1:n.-93+414_-93+418del
XM_006718003.2:c.-93+815_-93+819del	XP_006718066.1:n.-93+815_-93+819del
XM_011540233.1:c.-94+414_-94+418del	XP_011538535.1:n.-94+414_-94+418del
XM_011540234.1:c.-94+1317_-94+1321del	XP_011538536.1:n.-94+1317_-94+1321del
XM_011540235.1:c.-94+1248_-94+1252del	XP_011538537.1:n.-94+1248_-94+1252del
XM_011540236.1:c.-94+815_-94+819del	XP_011538538.1:n.-94+815_-94+819del
NM_001324347.1:c.-93+414_-93+418del	NP_001311276.1:n.-93+414_-93+418del
NM_001324348.1:c.-93+1248_-93+1252del	NP_001311277.1:n.-93+1248_-93+1252del
NM_001324349.1:c.-216+414_-216+418del	NP_001311278.1:n.-216+414_-216+418del
NM_001324350.1:c.-93+414_-93+418del	NP_001311279.1:n.-93+414_-93+418del
NM_001324351.1:c.-216+1248_-216+1252del	NP_001311280.1:n.-216+1248_-216+1252del
NM_001324352.1:c.-94+414_-94+418del	NP_001311281.1:n.-94+414_-94+418del
NM_001324353.1:c.15+414_15+418del	NP_001311282.1:n.15+414_15+418del
XM_006718003.3:c.-93+815_-93+819del	XP_006718066.1:n.-93+815_-93+819del
XM_011540232.3:c.-2833_-2829del	XP_011538534.1:n.-2833_-2829del
XM_011540234.2:c.-94+1317_-94+1321del	XP_011538536.1:n.-94+1317_-94+1321del
XM_011540235.2:c.-94+1248_-94+1252del	XP_011538537.1:n.-94+1248_-94+1252del
XM_011540236.2:c.-94+815_-94+819del	XP_011538538.1:n.-94+815_-94+819del
XM_017016740.1:c.-94+414_-94+418del	XP_016872229.1:n.-94+414_-94+418del
NM_001099282.2:c.-216+414_-216+418del MANE Select	NP_001092752.1:n.-216+414_-216+418del
NM_001324347.2:c.-93+414_-93+418del	NP_001311276.1:n.-93+414_-93+418del
NM_001324348.2:c.-93+1248_-93+1252del	NP_001311277.1:n.-93+1248_-93+1252del
NM_001324349.2:c.-216+414_-216+418del	NP_001311278.1:n.-216+414_-216+418del
NM_001324350.2:c.-93+414_-93+418del	NP_001311279.1:n.-93+414_-93+418del
NM_001324351.2:c.-216+1248_-216+1252del	NP_001311280.1:n.-216+1248_-216+1252del
NM_001324352.2:c.-94+414_-94+418del	NP_001311281.1:n.-94+414_-94+418del
NM_001324353.2:c.15+414_15+418del	NP_001311282.1:n.15+414_15+418del
NM_001099283.2:c.-93+1317_-93+1321del	NP_001092753.1:n.-93+1317_-93+1321del
NM_001099284.2:c.-216+1317_-216+1321del	NP_001092754.1:n.-216+1317_-216+1321del