Canonical Allele Identifier: CA1796999334
Gene: ZBTB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.80526262A= , CM000670.2:g.80526262A= GRCh38
NC_000008.10:g.81438497A= , CM000670.1:g.81438497A= GRCh37
NC_000008.9:g.81601052A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455036.8:c.*6734A= MANE Select ENSP00000412036.3:n.*6734A=
ENST00000426744.5:c.*6734A= ENSP00000416134.2:n.*6734A=
ENST00000430430.5:c.*6734A= ENSP00000387462.1:n.*6734A=
NM_001105539.2:c.*6734A= NP_001099009.1:n.*6734A=
NM_001277145.1:c.*6734A= NP_001264074.1:n.*6734A=
NM_023929.4:c.*6734A= NP_076418.3:n.*6734A=
XM_005251287.3:c.*6734A= XP_005251344.1:n.*6734A=
NM_001105539.3:c.*6734A= MANE Select NP_001099009.1:n.*6734A=
NM_001277145.2:c.*6734A= NP_001264074.1:n.*6734A=
NM_023929.5:c.*6734A= NP_076418.3:n.*6734A=