Canonical Allele Identifier: CA645584895
Gene: TSHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.81143108_81143109delinsAT , CM000676.2:g.81143108_81143109delinsAT GRCh38
NC_000014.8:g.81609452_81609453delinsAT , CM000676.1:g.81609452_81609453delinsAT GRCh37
NC_000014.7:g.80679205_80679206delinsAT NCBI36
NG_009206.1:g.192584_192585delinsAT , LRG_523:g.192584_192585delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000298171.7:c.1050_1051delinsAT MANE Select ENSP00000298171.2:p.His351Tyr
ENST00000636454.1:n.968_969delinsAT
ENST00000298171.6:c.1050_1051delinsAT ENSP00000298171.2:p.His351Tyr
ENST00000541158.6:c.1050_1051delinsAT ENSP00000441235.2:p.His351Tyr
NM_000369.2:c.1050_1051delinsAT , LRG_523t1:c.1050_1051delinsAT NP_000360.2:p.His351Tyr
XM_005268037.3:c.1050_1051delinsAT XP_005268094.1:p.His351Tyr
XM_011537119.1:c.771_772delinsAT XP_011535421.1:p.His258Tyr
XR_245790.3:n.2086+22084_2086+22085delinsAT
XR_429385.2:n.853+22084_853+22085delinsAT
XR_429386.2:n.854+22084_854+22085delinsAT
XR_944075.1:n.865+22084_865+22085delinsAT
XR_944076.1:n.861+22084_861+22085delinsAT
XR_944077.1:n.865+22084_865+22085delinsAT
XR_944078.1:n.865+22084_865+22085delinsAT
XR_944079.1:n.855+22084_855+22085delinsAT
XM_005268037.4:c.1050_1051delinsAT XP_005268094.1:p.His351Tyr
XM_011537119.2:c.771_772delinsAT XP_011535421.1:p.His258Tyr
XR_001751021.1:n.2753+22084_2753+22085delinsAT
XR_001751022.1:n.2753+22084_2753+22085delinsAT
XR_001751023.1:n.2753+22084_2753+22085delinsAT
XR_944075.3:n.929+22084_929+22085delinsAT
NM_000369.4:c.1050_1051delinsAT NP_000360.2:p.His351Tyr
NM_000369.5:c.1050_1051delinsAT MANE Select NP_000360.2:p.His351Tyr