Canonical Allele Identifier: CA2635847049
Gene: ZBTB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7459757del , CM000679.2:g.7459757del GRCh38
NC_000017.10:g.7363076del , CM000679.1:g.7363076del GRCh37
NC_000017.9:g.7303800del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380599.9:c.*2186del MANE Select ENSP00000369973.4:n.*2186del
ENST00000311403.4:c.*2186del ENSP00000307858.4:n.*2186del
ENST00000380599.8:c.*2186del ENSP00000369973.4:n.*2186del
NM_001128833.1:c.*2185del NP_001122305.1:n.*2185del
NM_020899.3:c.*2185del NP_065950.2:n.*2185del
XM_006721563.2:c.*2186del XP_006721626.1:n.*2186del
XM_006721564.1:c.*2186del XP_006721627.1:n.*2186del
XM_011523972.1:c.*2186del XP_011522274.1:n.*2186del
XM_006721563.3:c.*2186del XP_006721626.1:n.*2186del
XM_006721564.2:c.*2186del XP_006721627.1:n.*2186del
XM_011523972.2:c.*2186del XP_011522274.1:n.*2186del
NM_001128833.2:c.*2186del MANE Select NP_001122305.1:n.*2186del
NM_020899.4:c.*2186del NP_065950.2:n.*2186del