Canonical Allele Identifier: CA2512041889
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033538_115033539del , CM000663.2:g.115033538_115033539del GRCh38
NC_000001.10:g.115576159_115576160del , CM000663.1:g.115576159_115576160del GRCh37
NC_000001.9:g.115377682_115377683del NCBI36
NG_015891.1:g.8745_8746del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.162+14_162+15del MANE Select ENSP00000256592.1:n.162+14_162+15del
ENST00000256592.2:c.162+14_162+15del ENSP00000256592.1:n.162+14_162+15del
ENST00000369517.1:c.162+14_162+15del ENSP00000358530.1:n.162+14_162+15del
NM_000549.4:c.162+14_162+15del NP_000540.2:n.162+14_162+15del
XM_011542065.1:c.162+14_162+15del XP_011540367.1:n.162+14_162+15del
XM_011542065.2:c.162+14_162+15del XP_011540367.1:n.162+14_162+15del
NM_000549.5:c.162+14_162+15del MANE Select NP_000540.2:n.162+14_162+15del
Search 100 bp 5'
Search 100 bp 3'