Canonical Allele Identifier: CA2150074487
Gene: TSHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.81142952C= , CM000676.2:g.81142952C= GRCh38
NC_000014.8:g.81609296C= , CM000676.1:g.81609296C= GRCh37
NC_000014.7:g.80679049C= NCBI36
NG_009206.1:g.192428C= , LRG_523:g.192428C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298171.7:c.894C= MANE Select ENSP00000298171.2:p.Ser298=
ENST00000636454.1:n.812C=
ENST00000298171.6:c.894C= ENSP00000298171.2:p.Ser298=
ENST00000541158.6:c.894C= ENSP00000441235.2:p.Ser298=
NM_000369.2:c.894C= , LRG_523t1:c.894C= NP_000360.2:p.Ser298=
XM_005268037.3:c.894C= XP_005268094.1:p.Ser298=
XM_011537119.1:c.615C= XP_011535421.1:p.Ser205=
XR_245790.3:n.2086+22241G=
XR_429385.2:n.853+22241G=
XR_429386.2:n.854+22241G=
XR_944075.1:n.865+22241G=
XR_944076.1:n.861+22241G=
XR_944077.1:n.865+22241G=
XR_944078.1:n.865+22241G=
XR_944079.1:n.855+22241G=
XM_005268037.4:c.894C= XP_005268094.1:p.Ser298=
XM_011537119.2:c.615C= XP_011535421.1:p.Ser205=
XR_001751021.1:n.2753+22241G=
XR_001751022.1:n.2753+22241G=
XR_001751023.1:n.2753+22241G=
XR_944075.3:n.929+22241G=
NM_000369.4:c.894C= NP_000360.2:p.Ser298=
NM_000369.5:c.894C= MANE Select NP_000360.2:p.Ser298=