Canonical Allele Identifier: CA2150070465

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81092237C= , CM000676.2:g.81092237C=	GRCh38
NC_000014.8:g.81558581C= , CM000676.1:g.81558581C=	GRCh37
NC_000014.7:g.80628334C=	NCBI36
NG_009206.1:g.141713C= , LRG_523:g.141713C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.468-294C= MANE Select	ENSP00000298171.2:n.468-294C=
ENST00000636454.1:n.386-294C=
ENST00000298171.6:c.468-294C=	ENSP00000298171.2:n.468-294C=
ENST00000342443.10:c.468-294C=	ENSP00000340113.6:n.468-294C=
ENST00000541158.6:c.468-294C=	ENSP00000441235.2:n.468-294C=
ENST00000554263.5:c.468-294C=	ENSP00000451202.1:n.468-294C=
ENST00000554435.1:c.468-294C=	ENSP00000450549.1:n.468-294C=
NM_000369.2:c.468-294C= , LRG_523t1:c.468-294C=	NP_000360.2:n.468-294C=
NM_001018036.2:c.468-294C=	NP_001018046.1:n.468-294C=
NM_001142626.2:c.468-294C=	NP_001136098.1:n.468-294C=
XM_005268037.3:c.468-294C=	XP_005268094.1:n.468-294C=
XM_005268039.1:c.468-294C=	XP_005268096.1:n.468-294C=
XM_006720245.1:c.468-294C=	XP_006720308.1:n.468-294C=
XM_011537119.1:c.189-294C=	XP_011535421.1:n.189-294C=
XR_245790.3:n.2480+1345G=
XR_944075.1:n.1353+77G=
XR_944076.1:n.1255+1345G=
XR_944077.1:n.1259+1345G=
XR_944078.1:n.1259+1345G=
XM_005268037.4:c.468-294C=	XP_005268094.1:n.468-294C=
XM_011537119.2:c.189-294C=	XP_011535421.1:n.189-294C=
XR_001751018.2:n.793+77G=
XR_001751019.2:n.699+1345G=
XR_001751020.2:n.699+1345G=
XR_001751021.1:n.3241+77G=
XR_001751022.1:n.3147+1345G=
XR_001751023.1:n.3280+1345G=
XR_001751024.2:n.793+77G=
XR_944075.3:n.1417+77G=
NM_000369.4:c.468-294C=	NP_000360.2:n.468-294C=
NM_001018036.3:c.468-294C=	NP_001018046.1:n.468-294C=
NM_001142626.3:c.468-294C=	NP_001136098.1:n.468-294C=
NM_000369.5:c.468-294C= MANE Select	NP_000360.2:n.468-294C=