Canonical Allele Identifier: CA2590158730
Gene: ZBTB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7459657_7459662del , CM000679.2:g.7459657_7459662del GRCh38
NC_000017.10:g.7362976_7362981del , CM000679.1:g.7362976_7362981del GRCh37
NC_000017.9:g.7303700_7303705del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380599.9:c.*2279_*2284del MANE Select ENSP00000369973.4:n.*2279_*2284del
ENST00000311403.4:c.*2279_*2284del ENSP00000307858.4:n.*2279_*2284del
ENST00000380599.8:c.*2279_*2284del ENSP00000369973.4:n.*2279_*2284del
NM_001128833.1:c.*2278_*2283del NP_001122305.1:n.*2278_*2283del
NM_020899.3:c.*2278_*2283del NP_065950.2:n.*2278_*2283del
XM_006721563.2:c.*2279_*2284del XP_006721626.1:n.*2279_*2284del
XM_006721564.1:c.*2279_*2284del XP_006721627.1:n.*2279_*2284del
XM_011523972.1:c.*2279_*2284del XP_011522274.1:n.*2279_*2284del
XM_006721563.3:c.*2279_*2284del XP_006721626.1:n.*2279_*2284del
XM_006721564.2:c.*2279_*2284del XP_006721627.1:n.*2279_*2284del
XM_011523972.2:c.*2279_*2284del XP_011522274.1:n.*2279_*2284del
NM_001128833.2:c.*2279_*2284del MANE Select NP_001122305.1:n.*2279_*2284del
NM_020899.4:c.*2279_*2284del NP_065950.2:n.*2279_*2284del