Canonical Allele Identifier: CA2808375420

Gene: ZBTB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7459641T>G , CM000679.2:g.7459641T>G	GRCh38
NC_000017.10:g.7362960T>G , CM000679.1:g.7362960T>G	GRCh37
NC_000017.9:g.7303684T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000380599.9:c.*2299A>C MANE Select	ENSP00000369973.4:n.*2299A>C
ENST00000311403.4:c.*2299A>C	ENSP00000307858.4:n.*2299A>C
ENST00000380599.8:c.*2299A>C	ENSP00000369973.4:n.*2299A>C
NM_001128833.1:c.*2298A>C	NP_001122305.1:n.*2298A>C
NM_020899.3:c.*2298A>C	NP_065950.2:n.*2298A>C
XM_006721563.2:c.*2299A>C	XP_006721626.1:n.*2299A>C
XM_006721564.1:c.*2299A>C	XP_006721627.1:n.*2299A>C
XM_011523972.1:c.*2299A>C	XP_011522274.1:n.*2299A>C
XM_006721563.3:c.*2299A>C	XP_006721626.1:n.*2299A>C
XM_006721564.2:c.*2299A>C	XP_006721627.1:n.*2299A>C
XM_011523972.2:c.*2299A>C	XP_011522274.1:n.*2299A>C
NM_001128833.2:c.*2299A>C MANE Select	NP_001122305.1:n.*2299A>C
NM_020899.4:c.*2299A>C	NP_065950.2:n.*2299A>C