Canonical Allele Identifier: CA2802330141

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80996469_80996470insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC , CM000676.2:g.80996469_80996470insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	GRCh38
NC_000014.8:g.81462813_81462814insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC , CM000676.1:g.81462813_81462814insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	GRCh37
NC_000014.7:g.80532566_80532567insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	NCBI36
NG_009206.1:g.45945_45946insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC , LRG_523:g.45945_45946insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000298171.7:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC MANE Select	ENSP00000298171.2:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAA...
ENST00000298171.6:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	ENSP00000298171.2:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAA...
ENST00000342443.10:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	ENSP00000340113.6:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAA...
ENST00000541158.6:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	ENSP00000441235.2:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAA...
ENST00000553763.1:n.270+40619_270+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC
ENST00000554263.5:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	ENSP00000451202.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAA...
ENST00000554435.1:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	ENSP00000450549.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAA...
ENST00000555326.5:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	ENSP00000451092.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAA...
NM_000369.2:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC , LRG_523t1:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	NP_000360.2:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTA...
NM_001018036.2:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	NP_001018046.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
NM_001142626.2:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	NP_001136098.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
XM_005268037.3:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	XP_005268094.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
XM_005268039.1:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	XP_005268096.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
XM_006720245.1:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	XP_006720308.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
XM_011537119.1:c.-159+40619_-159+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	XP_011535421.1:n.-159+40619_-159+40620insCCTCTGCTGGTTAGCTGAAA...
XM_005268037.4:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	XP_005268094.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
XM_011537119.2:c.-159+40619_-159+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	XP_011535421.1:n.-159+40619_-159+40620insCCTCTGCTGGTTAGCTGAAA...
NM_000369.4:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	NP_000360.2:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTA...
NM_001018036.3:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	NP_001018046.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
NM_001142626.3:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC	NP_001136098.1:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGC...
NM_000369.5:c.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTAATCTGACAGAGCAAAGTGATTCAGAAAATTTTGCTC MANE Select	NP_000360.2:n.170+40619_170+40620insCCTCTGCTGGTTAGCTGAAAGCTTA...