Canonical Allele Identifier: CA2150055367
Gene: TSHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.81056784T>G , CM000676.2:g.81056784T>G GRCh38
NC_000014.8:g.81523128T>G , CM000676.1:g.81523128T>G GRCh37
NC_000014.7:g.80592881T>G NCBI36
NG_009206.1:g.106260T>G , LRG_523:g.106260T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298171.7:c.171-5364T>G MANE Select ENSP00000298171.2:n.171-5364T>G
ENST00000298171.6:c.171-5364T>G ENSP00000298171.2:n.171-5364T>G
ENST00000342443.10:c.171-5364T>G ENSP00000340113.6:n.171-5364T>G
ENST00000541158.6:c.171-5364T>G ENSP00000441235.2:n.171-5364T>G
ENST00000553763.1:n.271-5364T>G
ENST00000554263.5:c.171-5364T>G ENSP00000451202.1:n.171-5364T>G
ENST00000554435.1:c.171-5364T>G ENSP00000450549.1:n.171-5364T>G
ENST00000555326.5:c.171-5364T>G ENSP00000451092.1:n.171-5364T>G
NM_000369.2:c.171-5364T>G , LRG_523t1:c.171-5364T>G NP_000360.2:n.171-5364T>G
NM_001018036.2:c.171-5364T>G NP_001018046.1:n.171-5364T>G
NM_001142626.2:c.171-5364T>G NP_001136098.1:n.171-5364T>G
XM_005268037.3:c.171-5364T>G XP_005268094.1:n.171-5364T>G
XM_005268039.1:c.171-5364T>G XP_005268096.1:n.171-5364T>G
XM_006720245.1:c.171-5364T>G XP_006720308.1:n.171-5364T>G
XM_011537119.1:c.-158-5364T>G XP_011535421.1:n.-158-5364T>G
XR_245790.3:n.3676-2968A>C
XR_944075.1:n.2549-2968A>C
XR_944076.1:n.1442-2968A>C
XR_944077.1:n.2455-2968A>C
XR_944078.1:n.2455-2968A>C
XM_005268037.4:c.171-5364T>G XP_005268094.1:n.171-5364T>G
XM_011537119.2:c.-158-5364T>G XP_011535421.1:n.-158-5364T>G
XR_001751018.2:n.1989-2968A>C
XR_001751019.2:n.1895-2968A>C
XR_001751020.2:n.886-2968A>C
XR_001751021.1:n.4437-2968A>C
XR_001751022.1:n.3334-2968A>C
XR_001751023.1:n.4476-2968A>C
XR_001751024.2:n.1989-2968A>C
XR_944075.3:n.2613-2968A>C
NM_000369.4:c.171-5364T>G NP_000360.2:n.171-5364T>G
NM_001018036.3:c.171-5364T>G NP_001018046.1:n.171-5364T>G
NM_001142626.3:c.171-5364T>G NP_001136098.1:n.171-5364T>G
NM_000369.5:c.171-5364T>G MANE Select NP_000360.2:n.171-5364T>G