Canonical Allele Identifier: CA1190425268

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033603_115033614delinsGAAATAAATCAC , CM000663.2:g.115033603_115033614delinsGAAATAAATCAC	GRCh38
NC_000001.10:g.115576224_115576235delinsGAAATAAATCAC , CM000663.1:g.115576224_115576235delinsGAAATAAATCAC	GRCh37
NC_000001.9:g.115377747_115377758delinsGAAATAAATCAC	NCBI36
NG_015891.1:g.8810_8821delinsGAAATAAATCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+79_162+90delinsGAAATAAATCAC MANE Select	ENSP00000256592.1:n.162+79_162+90delinsGAAATAAATCAC
ENST00000256592.2:c.162+79_162+90delinsGAAATAAATCAC	ENSP00000256592.1:n.162+79_162+90delinsGAAATAAATCAC
ENST00000369517.1:c.162+79_162+90delinsGAAATAAATCAC	ENSP00000358530.1:n.162+79_162+90delinsGAAATAAATCAC
NM_000549.4:c.162+79_162+90delinsGAAATAAATCAC	NP_000540.2:n.162+79_162+90delinsGAAATAAATCAC
XM_011542065.1:c.162+79_162+90delinsGAAATAAATCAC	XP_011540367.1:n.162+79_162+90delinsGAAATAAATCAC
XM_011542065.2:c.162+79_162+90delinsGAAATAAATCAC	XP_011540367.1:n.162+79_162+90delinsGAAATAAATCAC
NM_000549.5:c.162+79_162+90delinsGAAATAAATCAC MANE Select	NP_000540.2:n.162+79_162+90delinsGAAATAAATCAC