Canonical Allele Identifier: CA1190425174
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033336_115033340delinsGTTCT , CM000663.2:g.115033336_115033340delinsGTTCT GRCh38
NC_000001.10:g.115575957_115575961delinsGTTCT , CM000663.1:g.115575957_115575961delinsGTTCT GRCh37
NC_000001.9:g.115377480_115377484delinsGTTCT NCBI36
NG_015891.1:g.8543_8547delinsGTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-26_-1-22delinsGTTCT MANE Select ENSP00000256592.1:n.-1-26_-1-22delinsGTTCT
ENST00000256592.2:c.-1-26_-1-22delinsGTTCT ENSP00000256592.1:n.-1-26_-1-22delinsGTTCT
NM_000549.4:c.-1-26_-1-22delinsGTTCT NP_000540.2:n.-1-26_-1-22delinsGTTCT
XM_011542065.1:c.-27_-23delinsGTTCT XP_011540367.1:n.-27_-23delinsGTTCT
XM_011542065.2:c.-27_-23delinsGTTCT XP_011540367.1:n.-27_-23delinsGTTCT
NM_000549.5:c.-1-26_-1-22delinsGTTCT MANE Select NP_000540.2:n.-1-26_-1-22delinsGTTCT
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