Canonical Allele Identifier: CA1809870447
Gene: TRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109097543_109097545delinsCAT , CM000670.2:g.109097543_109097545delinsCAT GRCh38
NC_000008.10:g.110109772_110109774delinsCAT , CM000670.1:g.110109772_110109774delinsCAT GRCh37
NC_000008.9:g.110178948_110178950delinsCAT NCBI36
NG_017161.1:g.15097_15099delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.789+9242_789+9244delinsCAT MANE Select ENSP00000430711.2:n.789+9242_789+9244delinsCAT
ENST00000311762.2:c.789+9242_789+9244delinsCAT ENSP00000309818.2:n.789+9242_789+9244delinsCAT
ENST00000518632.1:c.789+9242_789+9244delinsCAT ENSP00000430711.1:n.789+9242_789+9244delinsCAT
NM_003301.5:c.789+9242_789+9244delinsCAT NP_003292.1:n.789+9242_789+9244delinsCAT
XM_011517263.1:c.789+9242_789+9244delinsCAT XP_011515565.1:n.789+9242_789+9244delinsCAT
XM_011517263.2:c.789+9242_789+9244delinsCAT XP_011515565.1:n.789+9242_789+9244delinsCAT
NM_003301.7:c.789+9242_789+9244delinsCAT MANE Select NP_003292.1:n.789+9242_789+9244delinsCAT
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