Canonical Allele Identifier: CA2757987910

Gene: ZBTB20

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114350116dup , CM000665.2:g.114350116dup	GRCh38
NC_000003.11:g.114068963dup , CM000665.1:g.114068963dup	GRCh37
NC_000003.10:g.115551653dup	NCBI36
NG_052992.1:g.802167dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470311.6:c.1585+160dup	ENSP00000420684.2:n.1585+160dup
ENST00000474710.6:c.1804+160dup	ENSP00000419153.1:n.1804+160dup
ENST00000704358.1:c.1804+160dup	ENSP00000515869.1:n.1804+160dup
ENST00000704360.1:c.*119dup	ENSP00000515870.1:n.*119dup
ENST00000704361.1:n.2002+160dup
ENST00000357258.8:c.1585+160dup	ENSP00000349803.3:n.1585+160dup
ENST00000675478.1:c.1804+160dup MANE Select	ENSP00000501561.1:n.1804+160dup
ENST00000676079.1:c.1804+160dup	ENSP00000502480.1:n.1804+160dup
ENST00000357258.7:c.1585+160dup	ENSP00000349803.3:n.1585+160dup
ENST00000393785.6:c.1585+160dup	ENSP00000377375.2:n.1585+160dup
ENST00000462705.5:c.1585+160dup	ENSP00000420324.1:n.1585+160dup
ENST00000464560.5:c.1585+160dup	ENSP00000417307.1:n.1585+160dup
ENST00000471418.5:c.1585+160dup	ENSP00000419902.1:n.1585+160dup
ENST00000474710.5:c.1804+160dup	ENSP00000419153.1:n.1804+160dup
ENST00000479879.5:n.443-10688dup
ENST00000481632.5:c.1585+160dup	ENSP00000418092.1:n.1585+160dup
NM_001164342.2:c.1804+160dup	NP_001157814.1:n.1804+160dup
NM_001164343.2:c.1585+160dup	NP_001157815.1:n.1585+160dup
NM_001164344.2:c.1585+160dup	NP_001157816.1:n.1585+160dup
NM_001164345.2:c.1585+160dup	NP_001157817.1:n.1585+160dup
NM_001164346.2:c.1585+160dup	NP_001157818.1:n.1585+160dup
NM_001164347.2:c.1585+160dup	NP_001157819.1:n.1585+160dup
NM_015642.5:c.1585+160dup	NP_056457.3:n.1585+160dup
NR_121662.1:n.467-10688dup
NM_001348800.1:c.1804+160dup	NP_001335729.1:n.1804+160dup
NM_001348801.1:c.1585+160dup	NP_001335730.1:n.1585+160dup
NM_001348802.1:c.1585+160dup	NP_001335731.1:n.1585+160dup
NM_001348803.1:c.1804+160dup	NP_001335732.1:n.1804+160dup
NM_001348804.1:c.1585+160dup	NP_001335733.1:n.1585+160dup
NM_001348805.1:c.1585+160dup	NP_001335734.1:n.1585+160dup
NM_001164344.3:c.1585+160dup	NP_001157816.1:n.1585+160dup
NM_001164345.3:c.1585+160dup	NP_001157817.1:n.1585+160dup
NM_001348800.3:c.1804+160dup MANE Select	NP_001335729.1:n.1804+160dup
NM_001348801.2:c.1585+160dup	NP_001335730.1:n.1585+160dup
NM_001348802.2:c.1585+160dup	NP_001335731.1:n.1585+160dup
NM_001348803.2:c.1804+160dup	NP_001335732.1:n.1804+160dup
NM_001348804.2:c.1585+160dup	NP_001335733.1:n.1585+160dup
NM_001348805.2:c.1585+160dup	NP_001335734.1:n.1585+160dup
NM_015642.6:c.1585+160dup	NP_056457.3:n.1585+160dup
NR_121662.2:n.470-10688dup
NM_001164344.4:c.1585+160dup	NP_001157816.1:n.1585+160dup
NM_001164345.4:c.1585+160dup	NP_001157817.1:n.1585+160dup
NM_001348801.3:c.1585+160dup	NP_001335730.1:n.1585+160dup
NM_001348802.3:c.1585+160dup	NP_001335731.1:n.1585+160dup
NM_001348803.3:c.1804+160dup	NP_001335732.1:n.1804+160dup
NM_001348804.3:c.1585+160dup	NP_001335733.1:n.1585+160dup
NM_001348805.3:c.1585+160dup	NP_001335734.1:n.1585+160dup
NM_001393393.1:c.1804+160dup	NP_001380322.1:n.1804+160dup
NM_001393394.1:c.1804+160dup	NP_001380323.1:n.1804+160dup
NM_001393395.1:c.1585+160dup	NP_001380324.1:n.1585+160dup
NM_001393396.1:c.1585+160dup	NP_001380325.1:n.1585+160dup
NM_015642.7:c.1585+160dup	NP_056457.3:n.1585+160dup
NR_121662.3:n.470-10688dup