Canonical Allele Identifier: CA363465175

Gene: C2 ZBTB12

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31900525C>A , CM000668.2:g.31900525C>A	GRCh38
NC_000006.11:g.31868302C>A , CM000668.1:g.31868302C>A	GRCh37
NC_000006.10:g.31976281C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_181842.3:c.781G>T (ZBTB12) MANE Select	NP_862825.1:p.Gly261Cys
ENST00000375527.3:c.781G>T (ZBTB12) MANE Select	ENSP00000364677.2:p.Gly261Cys
NM_001282457.1:c.-64+2583C>A (C2)	NP_001269386.1:n.-64+2583C>A
NM_001282457.2:c.-64+2583C>A (C2)	NP_001269386.1:n.-64+2583C>A
NM_181842.2:c.781G>T (ZBTB12)	NP_862825.1:p.Gly261Cys
ENST00000375527.2:c.781G>T (ZBTB12)	ENSP00000364677.2:p.Gly261Cys
ENST00000469372.5:c.-64+2583C>A (C2)	ENSP00000418923.1:n.-64+2583C>A
ENST00000497706.5:c.-64+2583C>A (C2)	ENSP00000417482.1:n.-64+2583C>A
ENST00000497706.6:c.-64+2583C>A (C2)	ENSP00000417482.2:n.-64+2583C>A
ENST00000695637.1:c.-360+2250C>A (C2)	ENSP00000512074.1:n.-360+2250C>A
XM_011514383.1:c.892G>T (ZBTB12)	XP_011512685.1:p.Gly298Cys
XM_011514383.2:c.781G>T (ZBTB12)	XP_011512685.2:p.Gly261Cys