Canonical Allele Identifier: CA2586968541

Gene: ZBTB18

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244054400_244054401insTCTC , CM000663.2:g.244054400_244054401insTCTC	GRCh38
NC_000001.10:g.244217702_244217703insTCTC , CM000663.1:g.244217702_244217703insTCTC	GRCh37
NC_000001.9:g.242284325_242284326insTCTC	NCBI36
NG_033841.1:g.10462_10463insTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696615.1:c.599_600insTCTC	ENSP00000512755.1:p.Glu200AspfsTer?
ENST00000696616.1:c.599_600insTCTC	ENSP00000512756.1:p.Glu200AspfsTer?
ENST00000696617.1:c.*556_*557insTCTC	ENSP00000512757.1:n.*556_*557insTCTC
ENST00000696618.1:c.599_600insTCTC	ENSP00000512758.1:p.Glu200AspfsTer?
ENST00000358704.4:c.626_627insTCTC MANE Select	ENSP00000351539.4:p.Glu209AspfsTer?
ENST00000622512.1:c.599_600insTCTC	ENSP00000481278.1:p.Glu200AspfsTer?
NM_001278196.1:c.599_600insTCTC	NP_001265125.1:p.Glu200AspfsTer?
NM_006352.4:c.599_600insTCTC	NP_006343.2:p.Glu200AspfsTer?
NM_205768.2:c.626_627insTCTC	NP_991331.1:p.Glu209AspfsTer?
XM_005273006.2:c.599_600insTCTC	XP_005273063.1:p.Glu200AspfsTer?
XM_017000060.1:c.599_600insTCTC	XP_016855549.1:p.Glu200AspfsTer?
NM_001278196.2:c.599_600insTCTC	NP_001265125.1:p.Glu200AspfsTer?
NM_205768.3:c.626_627insTCTC MANE Select	NP_991331.1:p.Glu209AspfsTer?