Canonical Allele Identifier: CA2301693704

Gene: ZBTB7C

Linked Data

• dbSNP Id: rs11082671

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.48339226A>C , CM000680.2:g.48339226A>C	GRCh38
NC_000018.9:g.45865597A>C , CM000680.1:g.45865597A>C	GRCh37
NC_000018.8:g.44119595A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000590800.6:c.-303-828T>G MANE Select	ENSP00000467877.1:n.-303-828T>G
ENST00000586525.5:c.-206+70000T>G	ENSP00000468537.1:n.-206+70000T>G
ENST00000587107.5:c.-562-828T>G	ENSP00000465760.1:n.-562-828T>G
ENST00000588028.1:c.-432-828T>G	ENSP00000468152.1:n.-432-828T>G
ENST00000588053.5:c.-480-828T>G	ENSP00000466088.1:n.-480-828T>G
ENST00000588149.5:c.-435-828T>G	ENSP00000468814.1:n.-435-828T>G
ENST00000588566.5:c.-303-828T>G	ENSP00000467456.1:n.-303-828T>G
ENST00000588970.5:c.-454-828T>G	ENSP00000468502.1:n.-454-828T>G
ENST00000589170.5:c.-568-828T>G	ENSP00000467338.1:n.-568-828T>G
ENST00000589194.5:c.-583-828T>G	ENSP00000468019.1:n.-583-828T>G
ENST00000590178.5:c.-430-828T>G	ENSP00000465160.1:n.-430-828T>G
ENST00000590374.5:c.-558-828T>G	ENSP00000465494.1:n.-558-828T>G
ENST00000590800.5:c.-303-828T>G	ENSP00000467877.1:n.-303-828T>G
ENST00000590855.5:c.-430-828T>G	ENSP00000468306.1:n.-430-828T>G
ENST00000591279.5:c.-79+69132T>G	ENSP00000465265.1:n.-79+69132T>G
ENST00000591405.5:c.-303-828T>G	ENSP00000467758.1:n.-303-828T>G
ENST00000591526.5:c.-476-828T>G	ENSP00000468752.1:n.-476-828T>G
ENST00000592387.5:c.-256+70000T>G	ENSP00000465835.1:n.-256+70000T>G
ENST00000593159.5:c.-494-828T>G	ENSP00000465832.1:n.-494-828T>G
XM_005258227.2:c.-303-828T>G	XP_005258284.1:n.-303-828T>G
XM_005258229.3:c.-79+70000T>G	XP_005258286.1:n.-79+70000T>G
XM_011525863.1:c.-403-828T>G	XP_011524165.1:n.-403-828T>G
XM_011525864.1:c.-403-828T>G	XP_011524166.1:n.-403-828T>G
XM_011525865.1:c.-399-828T>G	XP_011524167.1:n.-399-828T>G
XM_011525867.1:c.-179+70000T>G	XP_011524169.1:n.-179+70000T>G
XM_011525870.1:c.-79+69132T>G	XP_011524172.1:n.-79+69132T>G
NM_001318841.1:c.-303-828T>G	NP_001305770.1:n.-303-828T>G
XM_005258229.4:c.-79+70000T>G	XP_005258286.1:n.-79+70000T>G
XM_011525861.2:c.-411-828T>G	XP_011524163.1:n.-411-828T>G
XM_011525863.3:c.-403-828T>G	XP_011524165.1:n.-403-828T>G
XM_011525864.2:c.-403-828T>G	XP_011524166.1:n.-403-828T>G
XM_011525865.3:c.-399-828T>G	XP_011524167.1:n.-399-828T>G
XM_011525869.3:c.-411-828T>G	XP_011524171.1:n.-411-828T>G
XM_011525870.2:c.-79+69132T>G	XP_011524172.1:n.-79+69132T>G
XM_017025605.1:c.-411-828T>G	XP_016881094.1:n.-411-828T>G
XM_017025606.2:c.-535-828T>G	XP_016881095.1:n.-535-828T>G
XM_017025607.1:c.-535-828T>G	XP_016881096.1:n.-535-828T>G
XM_017025608.1:c.-411-828T>G	XP_016881097.1:n.-411-828T>G
XM_017025609.2:c.-303-828T>G	XP_016881098.1:n.-303-828T>G
NM_001318841.2:c.-303-828T>G MANE Select	NP_001305770.1:n.-303-828T>G
NM_001371284.1:c.-558-828T>G	NP_001358213.1:n.-558-828T>G
NM_001371285.1:c.-256+70000T>G	NP_001358214.1:n.-256+70000T>G
NM_001371286.1:c.-79+69132T>G	NP_001358215.1:n.-79+69132T>G
NM_001371287.1:c.-435-828T>G	NP_001358216.1:n.-435-828T>G
NM_001371290.1:c.-568-828T>G	NP_001358219.1:n.-568-828T>G
NM_001371291.1:c.-432-828T>G	NP_001358220.1:n.-432-828T>G