Canonical Allele Identifier: CA2625933755
Gene: TSHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.81092606_81092618del , CM000676.2:g.81092606_81092618del GRCh38
NC_000014.8:g.81558950_81558962del , CM000676.1:g.81558950_81558962del GRCh37
NC_000014.7:g.80628703_80628715del NCBI36
NG_009206.1:g.142082_142094del , LRG_523:g.142082_142094del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298171.7:c.543_545+10del
ENST00000636454.1:n.461_463+10del
ENST00000298171.6:c.543_545+10del
ENST00000342443.10:c.543_545+10del
ENST00000541158.6:c.543_545+10del
ENST00000554263.5:c.543_545+10del
ENST00000554435.1:c.543_545+10del
NM_000369.2:c.543_545+10del , LRG_523t1:c.543_545+10del
NM_001018036.2:c.543_545+10del
NM_001142626.2:c.543_545+10del
XM_005268037.3:c.543_545+10del
XM_005268039.1:c.543_545+10del
XM_006720245.1:c.543_545+10del
XM_011537119.1:c.264_266+10del
XR_245790.3:n.2480+964_2480+976del
XR_944075.1:n.1260-211_1260-199del
XR_944076.1:n.1255+964_1255+976del
XR_944077.1:n.1259+964_1259+976del
XR_944078.1:n.1259+964_1259+976del
XM_005268037.4:c.543_545+10del
XM_011537119.2:c.264_266+10del
XR_001751018.2:n.700-211_700-199del
XR_001751019.2:n.699+964_699+976del
XR_001751020.2:n.699+964_699+976del
XR_001751021.1:n.3148-211_3148-199del
XR_001751022.1:n.3147+964_3147+976del
XR_001751023.1:n.3280+964_3280+976del
XR_001751024.2:n.700-211_700-199del
XR_944075.3:n.1324-211_1324-199del
NM_000369.4:c.543_545+10del
NM_001018036.3:c.543_545+10del
NM_001142626.3:c.543_545+10del
NM_000369.5:c.543_545+10del