Canonical Allele Identifier: CA1796999327

Gene: ZBTB10

Linked Data

• dbSNP Id: rs1816559663

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80526250dup , CM000670.2:g.80526250dup	GRCh38
NC_000008.10:g.81438485dup , CM000670.1:g.81438485dup	GRCh37
NC_000008.9:g.81601040dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455036.8:c.*6722dup MANE Select	ENSP00000412036.3:n.*6722dup
ENST00000426744.5:c.*6722dup	ENSP00000416134.2:n.*6722dup
ENST00000430430.5:c.*6722dup	ENSP00000387462.1:n.*6722dup
NM_001105539.2:c.*6722dup	NP_001099009.1:n.*6722dup
NM_001277145.1:c.*6722dup	NP_001264074.1:n.*6722dup
NM_023929.4:c.*6722dup	NP_076418.3:n.*6722dup
XM_005251287.3:c.*6722dup	XP_005251344.1:n.*6722dup
NM_001105539.3:c.*6722dup MANE Select	NP_001099009.1:n.*6722dup
NM_001277145.2:c.*6722dup	NP_001264074.1:n.*6722dup
NM_023929.5:c.*6722dup	NP_076418.3:n.*6722dup