Canonical Allele Identifier: CA1190425254

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033552_115033553delinsCT , CM000663.2:g.115033552_115033553delinsCT	GRCh38
NC_000001.10:g.115576173_115576174delinsCT , CM000663.1:g.115576173_115576174delinsCT	GRCh37
NC_000001.9:g.115377696_115377697delinsCT	NCBI36
NG_015891.1:g.8759_8760delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+28_162+29delinsCT MANE Select	ENSP00000256592.1:n.162+28_162+29delinsCT
ENST00000256592.2:c.162+28_162+29delinsCT	ENSP00000256592.1:n.162+28_162+29delinsCT
ENST00000369517.1:c.162+28_162+29delinsCT	ENSP00000358530.1:n.162+28_162+29delinsCT
NM_000549.4:c.162+28_162+29delinsCT	NP_000540.2:n.162+28_162+29delinsCT
XM_011542065.1:c.162+28_162+29delinsCT	XP_011540367.1:n.162+28_162+29delinsCT
XM_011542065.2:c.162+28_162+29delinsCT	XP_011540367.1:n.162+28_162+29delinsCT
NM_000549.5:c.162+28_162+29delinsCT MANE Select	NP_000540.2:n.162+28_162+29delinsCT