Canonical Allele Identifier: CA11595762

Gene: ZBTB20

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114643917C>G , CM000665.2:g.114643917C>G	GRCh38
NC_000003.11:g.114362764C>G , CM000665.1:g.114362764C>G	GRCh37
NC_000003.10:g.115845454C>G	NCBI36
NG_052992.1:g.508364G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474710.6:c.-475+49611G>C	ENSP00000419153.1:n.-475+49611G>C
ENST00000704358.1:c.-426+49611G>C	ENSP00000515869.1:n.-426+49611G>C
ENST00000704360.1:c.-350+49611G>C	ENSP00000515870.1:n.-350+49611G>C
ENST00000357258.8:c.-350+49611G>C	ENSP00000349803.3:n.-350+49611G>C
ENST00000675478.1:c.-295+49611G>C MANE Select	ENSP00000501561.1:n.-295+49611G>C
ENST00000357258.7:c.-350+49611G>C	ENSP00000349803.3:n.-350+49611G>C
ENST00000462705.5:c.-350+49611G>C	ENSP00000420324.1:n.-350+49611G>C
ENST00000463890.5:n.375+49611G>C
ENST00000464560.5:c.-350+49611G>C	ENSP00000417307.1:n.-350+49611G>C
ENST00000471418.5:c.-350+49611G>C	ENSP00000419902.1:n.-350+49611G>C
ENST00000479879.5:n.114-143526G>C
ENST00000480832.5:n.200+49611G>C
ENST00000491500.5:n.185+49611G>C
ENST00000492665.5:n.280-44571G>C
NM_001164343.2:c.-350+49611G>C	NP_001157815.1:n.-350+49611G>C
NM_001164344.2:c.-350+49611G>C	NP_001157816.1:n.-350+49611G>C
NM_001164345.2:c.-350+49611G>C	NP_001157817.1:n.-350+49611G>C
NM_015642.5:c.-350+49611G>C	NP_056457.3:n.-350+49611G>C
NR_121662.1:n.138-143526G>C
NM_001348800.1:c.-295+49611G>C	NP_001335729.1:n.-295+49611G>C
NM_001348801.1:c.-350+49611G>C	NP_001335730.1:n.-350+49611G>C
NM_001348802.1:c.-350+49611G>C	NP_001335731.1:n.-350+49611G>C
NM_001348803.1:c.-418+49611G>C	NP_001335732.1:n.-418+49611G>C
NM_001348804.1:c.-350+49611G>C	NP_001335733.1:n.-350+49611G>C
NM_001348805.1:c.-350+49611G>C	NP_001335734.1:n.-350+49611G>C
NM_001164344.3:c.-350+49611G>C	NP_001157816.1:n.-350+49611G>C
NM_001164345.3:c.-350+49611G>C	NP_001157817.1:n.-350+49611G>C
NM_001348800.3:c.-295+49611G>C MANE Select	NP_001335729.1:n.-295+49611G>C
NM_001348801.2:c.-350+49611G>C	NP_001335730.1:n.-350+49611G>C
NM_001348802.2:c.-350+49611G>C	NP_001335731.1:n.-350+49611G>C
NM_001348803.2:c.-418+49611G>C	NP_001335732.1:n.-418+49611G>C
NM_001348804.2:c.-350+49611G>C	NP_001335733.1:n.-350+49611G>C
NM_001348805.2:c.-350+49611G>C	NP_001335734.1:n.-350+49611G>C
NM_015642.6:c.-350+49611G>C	NP_056457.3:n.-350+49611G>C
NR_121662.2:n.141-143526G>C
NM_001164344.4:c.-350+49611G>C	NP_001157816.1:n.-350+49611G>C
NM_001164345.4:c.-350+49611G>C	NP_001157817.1:n.-350+49611G>C
NM_001348801.3:c.-350+49611G>C	NP_001335730.1:n.-350+49611G>C
NM_001348802.3:c.-350+49611G>C	NP_001335731.1:n.-350+49611G>C
NM_001348803.3:c.-418+49611G>C	NP_001335732.1:n.-418+49611G>C
NM_001348804.3:c.-350+49611G>C	NP_001335733.1:n.-350+49611G>C
NM_001348805.3:c.-350+49611G>C	NP_001335734.1:n.-350+49611G>C
NM_001393393.1:c.-295+49611G>C	NP_001380322.1:n.-295+49611G>C
NM_001393394.1:c.-361+49611G>C	NP_001380323.1:n.-361+49611G>C
NM_001393395.1:c.-350+49611G>C	NP_001380324.1:n.-350+49611G>C
NM_001393396.1:c.-350+49611G>C	NP_001380325.1:n.-350+49611G>C
NM_015642.7:c.-350+49611G>C	NP_056457.3:n.-350+49611G>C
NR_121662.3:n.141-143526G>C