Canonical Allele Identifier: CA2150070657

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81092668_81092673delinsATGTTT , CM000676.2:g.81092668_81092673delinsATGTTT	GRCh38
NC_000014.8:g.81559012_81559017delinsATGTTT , CM000676.1:g.81559012_81559017delinsATGTTT	GRCh37
NC_000014.7:g.80628765_80628770delinsATGTTT	NCBI36
NG_009206.1:g.142144_142149delinsATGTTT , LRG_523:g.142144_142149delinsATGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.545+60_545+65delinsATGTTT MANE Select	ENSP00000298171.2:n.545+60_545+65delinsATGTTT
ENST00000636454.1:n.463+60_463+65delinsATGTTT
ENST00000298171.6:c.545+60_545+65delinsATGTTT	ENSP00000298171.2:n.545+60_545+65delinsATGTTT
ENST00000342443.10:c.545+60_545+65delinsATGTTT	ENSP00000340113.6:n.545+60_545+65delinsATGTTT
ENST00000541158.6:c.545+60_545+65delinsATGTTT	ENSP00000441235.2:n.545+60_545+65delinsATGTTT
ENST00000554263.5:c.545+60_545+65delinsATGTTT	ENSP00000451202.1:n.545+60_545+65delinsATGTTT
ENST00000554435.1:c.545+60_545+65delinsATGTTT	ENSP00000450549.1:n.545+60_545+65delinsATGTTT
NM_000369.2:c.545+60_545+65delinsATGTTT , LRG_523t1:c.545+60_545+65delinsATGTTT	NP_000360.2:n.545+60_545+65delinsATGTTT
NM_001018036.2:c.545+60_545+65delinsATGTTT	NP_001018046.1:n.545+60_545+65delinsATGTTT
NM_001142626.2:c.545+60_545+65delinsATGTTT	NP_001136098.1:n.545+60_545+65delinsATGTTT
XM_005268037.3:c.545+60_545+65delinsATGTTT	XP_005268094.1:n.545+60_545+65delinsATGTTT
XM_005268039.1:c.545+60_545+65delinsATGTTT	XP_005268096.1:n.545+60_545+65delinsATGTTT
XM_006720245.1:c.545+60_545+65delinsATGTTT	XP_006720308.1:n.545+60_545+65delinsATGTTT
XM_011537119.1:c.266+60_266+65delinsATGTTT	XP_011535421.1:n.266+60_266+65delinsATGTTT
XR_245790.3:n.2480+909_2480+914delinsAAACAT
XR_944075.1:n.1260-266_1260-261delinsAAACAT
XR_944076.1:n.1255+909_1255+914delinsAAACAT
XR_944077.1:n.1259+909_1259+914delinsAAACAT
XR_944078.1:n.1259+909_1259+914delinsAAACAT
XM_005268037.4:c.545+60_545+65delinsATGTTT	XP_005268094.1:n.545+60_545+65delinsATGTTT
XM_011537119.2:c.266+60_266+65delinsATGTTT	XP_011535421.1:n.266+60_266+65delinsATGTTT
XR_001751018.2:n.700-266_700-261delinsAAACAT
XR_001751019.2:n.699+909_699+914delinsAAACAT
XR_001751020.2:n.699+909_699+914delinsAAACAT
XR_001751021.1:n.3148-266_3148-261delinsAAACAT
XR_001751022.1:n.3147+909_3147+914delinsAAACAT
XR_001751023.1:n.3280+909_3280+914delinsAAACAT
XR_001751024.2:n.700-266_700-261delinsAAACAT
XR_944075.3:n.1324-266_1324-261delinsAAACAT
NM_000369.4:c.545+60_545+65delinsATGTTT	NP_000360.2:n.545+60_545+65delinsATGTTT
NM_001018036.3:c.545+60_545+65delinsATGTTT	NP_001018046.1:n.545+60_545+65delinsATGTTT
NM_001142626.3:c.545+60_545+65delinsATGTTT	NP_001136098.1:n.545+60_545+65delinsATGTTT
NM_000369.5:c.545+60_545+65delinsATGTTT MANE Select	NP_000360.2:n.545+60_545+65delinsATGTTT