Canonical Allele Identifier: CA1144214954
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033903_115033905delinsTAT , CM000663.2:g.115033903_115033905delinsTAT GRCh38
NC_000001.10:g.115576524_115576526delinsTAT , CM000663.1:g.115576524_115576526delinsTAT GRCh37
NC_000001.9:g.115378047_115378049delinsTAT NCBI36
NG_015891.1:g.9110_9112delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-70_163-68delinsTAT MANE Select ENSP00000256592.1:n.163-70_163-68delinsTAT
ENST00000256592.2:c.163-70_163-68delinsTAT ENSP00000256592.1:n.163-70_163-68delinsTAT
ENST00000369517.1:c.163-70_163-68delinsTAT ENSP00000358530.1:n.163-70_163-68delinsTAT
NM_000549.4:c.163-70_163-68delinsTAT NP_000540.2:n.163-70_163-68delinsTAT
XM_011542065.1:c.163-70_163-68delinsTAT XP_011540367.1:n.163-70_163-68delinsTAT
XM_011542065.2:c.163-70_163-68delinsTAT XP_011540367.1:n.163-70_163-68delinsTAT
NM_000549.5:c.163-70_163-68delinsTAT MANE Select NP_000540.2:n.163-70_163-68delinsTAT