Canonical Allele Identifier: CA2245824286

Gene: ZBTB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7459548C= , CM000679.2:g.7459548C=	GRCh38
NC_000017.10:g.7362867C= , CM000679.1:g.7362867C=	GRCh37
NC_000017.9:g.7303591C=	NCBI36
NG_008026.1:g.19462C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380599.9:c.*2392G= MANE Select	ENSP00000369973.4:n.*2392G=
ENST00000311403.4:c.*2392G=	ENSP00000307858.4:n.*2392G=
ENST00000380599.8:c.*2392G=	ENSP00000369973.4:n.*2392G=
NM_001128833.1:c.*2391G=	NP_001122305.1:n.*2391G=
NM_020899.3:c.*2391G=	NP_065950.2:n.*2391G=
XM_006721563.2:c.*2392G=	XP_006721626.1:n.*2392G=
XM_006721564.1:c.*2392G=	XP_006721627.1:n.*2392G=
XM_011523972.1:c.*2392G=	XP_011522274.1:n.*2392G=
XM_006721563.3:c.*2392G=	XP_006721626.1:n.*2392G=
XM_006721564.2:c.*2392G=	XP_006721627.1:n.*2392G=
XM_011523972.2:c.*2392G=	XP_011522274.1:n.*2392G=
NM_001128833.2:c.*2392G= MANE Select	NP_001122305.1:n.*2392G=
NM_020899.4:c.*2392G=	NP_065950.2:n.*2392G=