Canonical Allele Identifier: CA2533318115
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033563_115033564insCACA , CM000663.2:g.115033563_115033564insCACA GRCh38
NC_000001.10:g.115576184_115576185insCACA , CM000663.1:g.115576184_115576185insCACA GRCh37
NC_000001.9:g.115377707_115377708insCACA NCBI36
NG_015891.1:g.8770_8771insCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.162+39_162+40insCACA MANE Select ENSP00000256592.1:n.162+39_162+40insCACA
ENST00000256592.2:c.162+39_162+40insCACA ENSP00000256592.1:n.162+39_162+40insCACA
ENST00000369517.1:c.162+39_162+40insCACA ENSP00000358530.1:n.162+39_162+40insCACA
NM_000549.4:c.162+39_162+40insCACA NP_000540.2:n.162+39_162+40insCACA
XM_011542065.1:c.162+39_162+40insCACA XP_011540367.1:n.162+39_162+40insCACA
XM_011542065.2:c.162+39_162+40insCACA XP_011540367.1:n.162+39_162+40insCACA
NM_000549.5:c.162+39_162+40insCACA MANE Select NP_000540.2:n.162+39_162+40insCACA
Search 100 bp 5'
Search 100 bp 3'