Canonical Allele Identifier: CA1796999293

Gene: ZBTB10

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.80526185C= , CM000670.2:g.80526185C=	GRCh38
NC_000008.10:g.81438420C= , CM000670.1:g.81438420C=	GRCh37
NC_000008.9:g.81600975C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455036.8:c.*6657C= MANE Select	ENSP00000412036.3:n.*6657C=
ENST00000426744.5:c.*6657C=	ENSP00000416134.2:n.*6657C=
ENST00000430430.5:c.*6657C=	ENSP00000387462.1:n.*6657C=
NM_001105539.2:c.*6657C=	NP_001099009.1:n.*6657C=
NM_001277145.1:c.*6657C=	NP_001264074.1:n.*6657C=
NM_023929.4:c.*6657C=	NP_076418.3:n.*6657C=
XM_005251287.3:c.*6657C=	XP_005251344.1:n.*6657C=
NM_001105539.3:c.*6657C= MANE Select	NP_001099009.1:n.*6657C=
NM_001277145.2:c.*6657C=	NP_001264074.1:n.*6657C=
NM_023929.5:c.*6657C=	NP_076418.3:n.*6657C=