Canonical Allele Identifier: CA2506161476

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033576_115033577insCCC , CM000663.2:g.115033576_115033577insCCC	GRCh38
NC_000001.10:g.115576197_115576198insCCC , CM000663.1:g.115576197_115576198insCCC	GRCh37
NC_000001.9:g.115377720_115377721insCCC	NCBI36
NG_015891.1:g.8783_8784insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+52_162+53insCCC MANE Select	ENSP00000256592.1:n.162+52_162+53insCCC
ENST00000256592.2:c.162+52_162+53insCCC	ENSP00000256592.1:n.162+52_162+53insCCC
ENST00000369517.1:c.162+52_162+53insCCC	ENSP00000358530.1:n.162+52_162+53insCCC
NM_000549.4:c.162+52_162+53insCCC	NP_000540.2:n.162+52_162+53insCCC
XM_011542065.1:c.162+52_162+53insCCC	XP_011540367.1:n.162+52_162+53insCCC
XM_011542065.2:c.162+52_162+53insCCC	XP_011540367.1:n.162+52_162+53insCCC
NM_000549.5:c.162+52_162+53insCCC MANE Select	NP_000540.2:n.162+52_162+53insCCC