Canonical Allele Identifier: CA1796999306
Gene: ZBTB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80526202A= , CM000670.2:g.80526202A= GRCh38
NC_000008.10:g.81438437A= , CM000670.1:g.81438437A= GRCh37
NC_000008.9:g.81600992A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455036.8:c.*6674A= MANE Select ENSP00000412036.3:n.*6674A=
ENST00000426744.5:c.*6674A= ENSP00000416134.2:n.*6674A=
ENST00000430430.5:c.*6674A= ENSP00000387462.1:n.*6674A=
NM_001105539.2:c.*6674A= NP_001099009.1:n.*6674A=
NM_001277145.1:c.*6674A= NP_001264074.1:n.*6674A=
NM_023929.4:c.*6674A= NP_076418.3:n.*6674A=
XM_005251287.3:c.*6674A= XP_005251344.1:n.*6674A=
NM_001105539.3:c.*6674A= MANE Select NP_001099009.1:n.*6674A=
NM_001277145.2:c.*6674A= NP_001264074.1:n.*6674A=
NM_023929.5:c.*6674A= NP_076418.3:n.*6674A=