Canonical Allele Identifier: CA2647270497
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033900_115033905del , CM000663.2:g.115033900_115033905del GRCh38
NC_000001.10:g.115576521_115576526del , CM000663.1:g.115576521_115576526del GRCh37
NC_000001.9:g.115378044_115378049del NCBI36
NG_015891.1:g.9107_9112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-73_163-68del MANE Select ENSP00000256592.1:n.163-73_163-68del
ENST00000256592.2:c.163-73_163-68del ENSP00000256592.1:n.163-73_163-68del
ENST00000369517.1:c.163-73_163-68del ENSP00000358530.1:n.163-73_163-68del
NM_000549.4:c.163-73_163-68del NP_000540.2:n.163-73_163-68del
XM_011542065.1:c.163-73_163-68del XP_011540367.1:n.163-73_163-68del
XM_011542065.2:c.163-73_163-68del XP_011540367.1:n.163-73_163-68del
NM_000549.5:c.163-73_163-68del MANE Select NP_000540.2:n.163-73_163-68del