Canonical Allele Identifier: CA1796999266

Gene: ZBTB10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80526135T= , CM000670.2:g.80526135T=	GRCh38
NC_000008.10:g.81438370T= , CM000670.1:g.81438370T=	GRCh37
NC_000008.9:g.81600925T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455036.8:c.*6607T= MANE Select	ENSP00000412036.3:n.*6607T=
ENST00000426744.5:c.*6607T=	ENSP00000416134.2:n.*6607T=
ENST00000430430.5:c.*6607T=	ENSP00000387462.1:n.*6607T=
NM_001105539.2:c.*6607T=	NP_001099009.1:n.*6607T=
NM_001277145.1:c.*6607T=	NP_001264074.1:n.*6607T=
NM_023929.4:c.*6607T=	NP_076418.3:n.*6607T=
XM_005251287.3:c.*6607T=	XP_005251344.1:n.*6607T=
NM_001105539.3:c.*6607T= MANE Select	NP_001099009.1:n.*6607T=
NM_001277145.2:c.*6607T=	NP_001264074.1:n.*6607T=
NM_023929.5:c.*6607T=	NP_076418.3:n.*6607T=