Canonical Allele Identifier: CA401812076

Gene: ZBTB14

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5291631T>A , CM000680.2:g.5291631T>A	GRCh38
NC_000018.9:g.5291630T>A , CM000680.1:g.5291630T>A	GRCh37
NC_000018.8:g.5281630T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001243702.2:c.577A>T MANE Select	NP_001230631.1:p.Thr193Ser
ENST00000651870.1:c.577A>T MANE Select	ENSP00000499212.1:p.Thr193Ser
NM_001143823.2:c.577A>T	NP_001137295.1:p.Thr193Ser
NM_001143823.3:c.577A>T	NP_001137295.1:p.Thr193Ser
NM_001243702.1:c.577A>T	NP_001230631.1:p.Thr193Ser
NM_001243704.1:c.577A>T	NP_001230633.1:p.Thr193Ser
NM_001243704.2:c.577A>T	NP_001230633.1:p.Thr193Ser
NM_003409.4:c.577A>T	NP_003400.2:p.Thr193Ser
NM_003409.5:c.577A>T	NP_003400.2:p.Thr193Ser
ENST00000357006.8:c.577A>T	ENSP00000349503.4:p.Thr193Ser
ENST00000400143.7:c.577A>T	ENSP00000383009.3:p.Thr193Ser
ENST00000582388.5:c.577A>T	ENSP00000463555.1:p.Thr193Ser
ENST00000614697.4:c.577A>T	ENSP00000484129.1:p.Thr193Ser
ENST00000615385.4:c.577A>T	ENSP00000478971.1:p.Thr193Ser
XM_024451261.1:c.577A>T	XP_024307029.1:p.Thr193Ser
XM_024451262.1:c.577A>T	XP_024307030.1:p.Thr193Ser
XM_024451263.1:c.577A>T	XP_024307031.1:p.Thr193Ser
XM_024451264.1:c.577A>T	XP_024307032.1:p.Thr193Ser
XM_024451265.1:c.577A>T	XP_024307033.1:p.Thr193Ser
XM_024451266.1:c.577A>T	XP_024307034.1:p.Thr193Ser