Canonical Allele Identifier: CA855800919

Gene: ZBTB10

Linked Data

• dbSNP Id: rs1395012096
• gnomAD v3: 8-80526131-A-AT
• gnomAD v4: 8-80526131-A-AT
• MyVariant Identifiers: chr8:g.81438366_81438367insT (hg19) ; chr8:g.80526131_80526132insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80526131_80526132insT , CM000670.2:g.80526131_80526132insT	GRCh38
NC_000008.10:g.81438366_81438367insT , CM000670.1:g.81438366_81438367insT	GRCh37
NC_000008.9:g.81600921_81600922insT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455036.8:c.*6603_*6604insT MANE Select	ENSP00000412036.3:n.*6603_*6604insT
ENST00000426744.5:c.*6603_*6604insT	ENSP00000416134.2:n.*6603_*6604insT
ENST00000430430.5:c.*6603_*6604insT	ENSP00000387462.1:n.*6603_*6604insT
NM_001105539.2:c.*6603_*6604insT	NP_001099009.1:n.*6603_*6604insT
NM_001277145.1:c.*6603_*6604insT	NP_001264074.1:n.*6603_*6604insT
NM_023929.4:c.*6603_*6604insT	NP_076418.3:n.*6603_*6604insT
XM_005251287.3:c.*6603_*6604insT	XP_005251344.1:n.*6603_*6604insT
NM_001105539.3:c.*6603_*6604insT MANE Select	NP_001099009.1:n.*6603_*6604insT
NM_001277145.2:c.*6603_*6604insT	NP_001264074.1:n.*6603_*6604insT
NM_023929.5:c.*6603_*6604insT	NP_076418.3:n.*6603_*6604insT