Canonical Allele Identifier: CA2647270365

Gene: TSHB

Linked Data

• gnomAD v4: 1-115033559-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033564_115033565del , CM000663.2:g.115033564_115033565del	GRCh38
NC_000001.10:g.115576185_115576186del , CM000663.1:g.115576185_115576186del	GRCh37
NC_000001.9:g.115377708_115377709del	NCBI36
NG_015891.1:g.8771_8772del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+40_162+41del MANE Select	ENSP00000256592.1:n.162+40_162+41del
ENST00000256592.2:c.162+40_162+41del	ENSP00000256592.1:n.162+40_162+41del
ENST00000369517.1:c.162+40_162+41del	ENSP00000358530.1:n.162+40_162+41del
NM_000549.4:c.162+40_162+41del	NP_000540.2:n.162+40_162+41del
XM_011542065.1:c.162+40_162+41del	XP_011540367.1:n.162+40_162+41del
XM_011542065.2:c.162+40_162+41del	XP_011540367.1:n.162+40_162+41del
NM_000549.5:c.162+40_162+41del MANE Select	NP_000540.2:n.162+40_162+41del