Canonical Allele Identifier: CA2540664276

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033591_115033592insCC , CM000663.2:g.115033591_115033592insCC	GRCh38
NC_000001.10:g.115576212_115576213insCC , CM000663.1:g.115576212_115576213insCC	GRCh37
NC_000001.9:g.115377735_115377736insCC	NCBI36
NG_015891.1:g.8798_8799insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+67_162+68insCC MANE Select	ENSP00000256592.1:n.162+67_162+68insCC
ENST00000256592.2:c.162+67_162+68insCC	ENSP00000256592.1:n.162+67_162+68insCC
ENST00000369517.1:c.162+67_162+68insCC	ENSP00000358530.1:n.162+67_162+68insCC
NM_000549.4:c.162+67_162+68insCC	NP_000540.2:n.162+67_162+68insCC
XM_011542065.1:c.162+67_162+68insCC	XP_011540367.1:n.162+67_162+68insCC
XM_011542065.2:c.162+67_162+68insCC	XP_011540367.1:n.162+67_162+68insCC
NM_000549.5:c.162+67_162+68insCC MANE Select	NP_000540.2:n.162+67_162+68insCC