Canonical Allele Identifier: CA2150026426

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80984599_80984600delinsCT , CM000676.2:g.80984599_80984600delinsCT	GRCh38
NC_000014.8:g.81450943_81450944delinsCT , CM000676.1:g.81450943_81450944delinsCT	GRCh37
NC_000014.7:g.80520696_80520697delinsCT	NCBI36
NG_009206.1:g.34075_34076delinsCT , LRG_523:g.34075_34076delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.170+28749_170+28750delinsCT MANE Select	ENSP00000298171.2:n.170+28749_170+28750delinsCT
ENST00000642209.1:c.171-6942_171-6941delinsCT	ENSP00000495625.1:n.171-6942_171-6941delinsCT
ENST00000298171.6:c.170+28749_170+28750delinsCT	ENSP00000298171.2:n.170+28749_170+28750delinsCT
ENST00000342443.10:c.170+28749_170+28750delinsCT	ENSP00000340113.6:n.170+28749_170+28750delinsCT
ENST00000541158.6:c.170+28749_170+28750delinsCT	ENSP00000441235.2:n.170+28749_170+28750delinsCT
ENST00000553763.1:n.270+28749_270+28750delinsCT
ENST00000554263.5:c.170+28749_170+28750delinsCT	ENSP00000451202.1:n.170+28749_170+28750delinsCT
ENST00000554435.1:c.170+28749_170+28750delinsCT	ENSP00000450549.1:n.170+28749_170+28750delinsCT
ENST00000555326.5:c.170+28749_170+28750delinsCT	ENSP00000451092.1:n.170+28749_170+28750delinsCT
NM_000369.2:c.170+28749_170+28750delinsCT , LRG_523t1:c.170+28749_170+28750delinsCT	NP_000360.2:n.170+28749_170+28750delinsCT
NM_001018036.2:c.170+28749_170+28750delinsCT	NP_001018046.1:n.170+28749_170+28750delinsCT
NM_001142626.2:c.170+28749_170+28750delinsCT	NP_001136098.1:n.170+28749_170+28750delinsCT
XM_005268037.3:c.170+28749_170+28750delinsCT	XP_005268094.1:n.170+28749_170+28750delinsCT
XM_005268039.1:c.170+28749_170+28750delinsCT	XP_005268096.1:n.170+28749_170+28750delinsCT
XM_006720245.1:c.170+28749_170+28750delinsCT	XP_006720308.1:n.170+28749_170+28750delinsCT
XM_011537119.1:c.-159+28749_-159+28750delinsCT	XP_011535421.1:n.-159+28749_-159+28750delinsCT
XM_005268037.4:c.170+28749_170+28750delinsCT	XP_005268094.1:n.170+28749_170+28750delinsCT
XM_011537119.2:c.-159+28749_-159+28750delinsCT	XP_011535421.1:n.-159+28749_-159+28750delinsCT
NM_000369.4:c.170+28749_170+28750delinsCT	NP_000360.2:n.170+28749_170+28750delinsCT
NM_001018036.3:c.170+28749_170+28750delinsCT	NP_001018046.1:n.170+28749_170+28750delinsCT
NM_001142626.3:c.170+28749_170+28750delinsCT	NP_001136098.1:n.170+28749_170+28750delinsCT
NM_000369.5:c.170+28749_170+28750delinsCT MANE Select	NP_000360.2:n.170+28749_170+28750delinsCT