Canonical Allele Identifier: CA354005638

Gene: ZBTB20

Linked Data

• MyVariant Identifiers: chr3:g.114069135A>C (hg19) ; chr3:g.114350288A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114350288A>C , CM000665.2:g.114350288A>C	GRCh38
NC_000003.11:g.114069135A>C , CM000665.1:g.114069135A>C	GRCh37
NC_000003.10:g.115551825A>C	NCBI36
NG_052992.1:g.801993T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470311.6:c.1571T>G	ENSP00000420684.2:p.Met524Arg
ENST00000474710.6:c.1790T>G	ENSP00000419153.1:p.Met597Arg
ENST00000704358.1:c.1790T>G	ENSP00000515869.1:p.Met597Arg
ENST00000704360.1:c.1571T>G	ENSP00000515870.1:p.Met524Arg
ENST00000704361.1:n.1988T>G
ENST00000357258.8:c.1571T>G	ENSP00000349803.3:p.Met524Arg
ENST00000675478.1:c.1790T>G MANE Select	ENSP00000501561.1:p.Met597Arg
ENST00000676079.1:c.1790T>G	ENSP00000502480.1:p.Met597Arg
ENST00000357258.7:c.1571T>G	ENSP00000349803.3:p.Met524Arg
ENST00000393785.6:c.1571T>G	ENSP00000377375.2:p.Met524Arg
ENST00000462705.5:c.1571T>G	ENSP00000420324.1:p.Met524Arg
ENST00000464560.5:c.1571T>G	ENSP00000417307.1:p.Met524Arg
ENST00000471418.5:c.1571T>G	ENSP00000419902.1:p.Met524Arg
ENST00000474710.5:c.1790T>G	ENSP00000419153.1:p.Met597Arg
ENST00000479879.5:n.443-10862T>G
ENST00000481632.5:c.1571T>G	ENSP00000418092.1:p.Met524Arg
NM_001164342.2:c.1790T>G	NP_001157814.1:p.Met597Arg
NM_001164343.2:c.1571T>G	NP_001157815.1:p.Met524Arg
NM_001164344.2:c.1571T>G	NP_001157816.1:p.Met524Arg
NM_001164345.2:c.1571T>G	NP_001157817.1:p.Met524Arg
NM_001164346.2:c.1571T>G	NP_001157818.1:p.Met524Arg
NM_001164347.2:c.1571T>G	NP_001157819.1:p.Met524Arg
NM_015642.5:c.1571T>G	NP_056457.3:p.Met524Arg
NR_121662.1:n.467-10862T>G
NM_001348800.1:c.1790T>G	NP_001335729.1:p.Met597Arg
NM_001348801.1:c.1571T>G	NP_001335730.1:p.Met524Arg
NM_001348802.1:c.1571T>G	NP_001335731.1:p.Met524Arg
NM_001348803.1:c.1790T>G	NP_001335732.1:p.Met597Arg
NM_001348804.1:c.1571T>G	NP_001335733.1:p.Met524Arg
NM_001348805.1:c.1571T>G	NP_001335734.1:p.Met524Arg
NM_001164344.3:c.1571T>G	NP_001157816.1:p.Met524Arg
NM_001164345.3:c.1571T>G	NP_001157817.1:p.Met524Arg
NM_001348800.3:c.1790T>G MANE Select	NP_001335729.1:p.Met597Arg
NM_001348801.2:c.1571T>G	NP_001335730.1:p.Met524Arg
NM_001348802.2:c.1571T>G	NP_001335731.1:p.Met524Arg
NM_001348803.2:c.1790T>G	NP_001335732.1:p.Met597Arg
NM_001348804.2:c.1571T>G	NP_001335733.1:p.Met524Arg
NM_001348805.2:c.1571T>G	NP_001335734.1:p.Met524Arg
NM_015642.6:c.1571T>G	NP_056457.3:p.Met524Arg
NR_121662.2:n.470-10862T>G
NM_001164344.4:c.1571T>G	NP_001157816.1:p.Met524Arg
NM_001164345.4:c.1571T>G	NP_001157817.1:p.Met524Arg
NM_001348801.3:c.1571T>G	NP_001335730.1:p.Met524Arg
NM_001348802.3:c.1571T>G	NP_001335731.1:p.Met524Arg
NM_001348803.3:c.1790T>G	NP_001335732.1:p.Met597Arg
NM_001348804.3:c.1571T>G	NP_001335733.1:p.Met524Arg
NM_001348805.3:c.1571T>G	NP_001335734.1:p.Met524Arg
NM_001393393.1:c.1790T>G	NP_001380322.1:p.Met597Arg
NM_001393394.1:c.1790T>G	NP_001380323.1:p.Met597Arg
NM_001393395.1:c.1571T>G	NP_001380324.1:p.Met524Arg
NM_001393396.1:c.1571T>G	NP_001380325.1:p.Met524Arg
NM_015642.7:c.1571T>G	NP_056457.3:p.Met524Arg
NR_121662.3:n.470-10862T>G