Canonical Allele Identifier: CA2647270344

Gene: TSHB

Linked Data

• gnomAD v4: 1-115033387-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033388del , CM000663.2:g.115033388del	GRCh38
NC_000001.10:g.115576009del , CM000663.1:g.115576009del	GRCh37
NC_000001.9:g.115377532del	NCBI36
NG_015891.1:g.8595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.26del MANE Select	ENSP00000256592.1:p.Met9SerfsTer?
ENST00000256592.2:c.26del	ENSP00000256592.1:p.Met9SerfsTer?
ENST00000369517.1:c.26del	ENSP00000358530.1:p.Met9SerfsTer?
NM_000549.4:c.26del	NP_000540.2:p.Met9SerfsTer?
XM_011542065.1:c.26del	XP_011540367.1:p.Met9SerfsTer?
XM_011542065.2:c.26del	XP_011540367.1:p.Met9SerfsTer?
NM_000549.5:c.26del MANE Select	NP_000540.2:p.Met9SerfsTer?