Canonical Allele Identifier: CA2245824332
Gene: ZBTB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7459649C= , CM000679.2:g.7459649C= GRCh38
NC_000017.10:g.7362968C= , CM000679.1:g.7362968C= GRCh37
NC_000017.9:g.7303692C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380599.9:c.*2291G= MANE Select ENSP00000369973.4:n.*2291G=
ENST00000311403.4:c.*2291G= ENSP00000307858.4:n.*2291G=
ENST00000380599.8:c.*2291G= ENSP00000369973.4:n.*2291G=
NM_001128833.1:c.*2290G= NP_001122305.1:n.*2290G=
NM_020899.3:c.*2290G= NP_065950.2:n.*2290G=
XM_006721563.2:c.*2291G= XP_006721626.1:n.*2291G=
XM_006721564.1:c.*2291G= XP_006721627.1:n.*2291G=
XM_011523972.1:c.*2291G= XP_011522274.1:n.*2291G=
XM_006721563.3:c.*2291G= XP_006721626.1:n.*2291G=
XM_006721564.2:c.*2291G= XP_006721627.1:n.*2291G=
XM_011523972.2:c.*2291G= XP_011522274.1:n.*2291G=
NM_001128833.2:c.*2291G= MANE Select NP_001122305.1:n.*2291G=
NM_020899.4:c.*2291G= NP_065950.2:n.*2291G=