Canonical Allele Identifier: CA2563990448

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033561_115033562insGA , CM000663.2:g.115033561_115033562insGA	GRCh38
NC_000001.10:g.115576182_115576183insGA , CM000663.1:g.115576182_115576183insGA	GRCh37
NC_000001.9:g.115377705_115377706insGA	NCBI36
NG_015891.1:g.8768_8769insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+37_162+38insGA MANE Select	ENSP00000256592.1:n.162+37_162+38insGA
ENST00000256592.2:c.162+37_162+38insGA	ENSP00000256592.1:n.162+37_162+38insGA
ENST00000369517.1:c.162+37_162+38insGA	ENSP00000358530.1:n.162+37_162+38insGA
NM_000549.4:c.162+37_162+38insGA	NP_000540.2:n.162+37_162+38insGA
XM_011542065.1:c.162+37_162+38insGA	XP_011540367.1:n.162+37_162+38insGA
XM_011542065.2:c.162+37_162+38insGA	XP_011540367.1:n.162+37_162+38insGA
NM_000549.5:c.162+37_162+38insGA MANE Select	NP_000540.2:n.162+37_162+38insGA