Canonical Allele Identifier: CA2508022051

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033585_115033586del , CM000663.2:g.115033585_115033586del	GRCh38
NC_000001.10:g.115576206_115576207del , CM000663.1:g.115576206_115576207del	GRCh37
NC_000001.9:g.115377729_115377730del	NCBI36
NG_015891.1:g.8792_8793del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+61_162+62del MANE Select	ENSP00000256592.1:n.162+61_162+62del
ENST00000256592.2:c.162+61_162+62del	ENSP00000256592.1:n.162+61_162+62del
ENST00000369517.1:c.162+61_162+62del	ENSP00000358530.1:n.162+61_162+62del
NM_000549.4:c.162+61_162+62del	NP_000540.2:n.162+61_162+62del
XM_011542065.1:c.162+61_162+62del	XP_011540367.1:n.162+61_162+62del
XM_011542065.2:c.162+61_162+62del	XP_011540367.1:n.162+61_162+62del
NM_000549.5:c.162+61_162+62del MANE Select	NP_000540.2:n.162+61_162+62del