Canonical Allele Identifier: CA2150070604

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81092568G= , CM000676.2:g.81092568G=	GRCh38
NC_000014.8:g.81558912G= , CM000676.1:g.81558912G=	GRCh37
NC_000014.7:g.80628665G=	NCBI36
NG_009206.1:g.142044G= , LRG_523:g.142044G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.505G= MANE Select	ENSP00000298171.2:p.Val169=
ENST00000636454.1:n.423G=
ENST00000298171.6:c.505G=	ENSP00000298171.2:p.Val169=
ENST00000342443.10:c.505G=	ENSP00000340113.6:p.Val169=
ENST00000541158.6:c.505G=	ENSP00000441235.2:p.Val169=
ENST00000554263.5:c.505G=	ENSP00000451202.1:p.Val169=
ENST00000554435.1:c.505G=	ENSP00000450549.1:p.Val169=
NM_000369.2:c.505G= , LRG_523t1:c.505G=	NP_000360.2:p.Val169=
NM_001018036.2:c.505G=	NP_001018046.1:p.Val169=
NM_001142626.2:c.505G=	NP_001136098.1:p.Val169=
XM_005268037.3:c.505G=	XP_005268094.1:p.Val169=
XM_005268039.1:c.505G=	XP_005268096.1:p.Val169=
XM_006720245.1:c.505G=	XP_006720308.1:p.Val169=
XM_011537119.1:c.226G=	XP_011535421.1:p.Val76=
XR_245790.3:n.2480+1014C=
XR_944075.1:n.1260-161C=
XR_944076.1:n.1255+1014C=
XR_944077.1:n.1259+1014C=
XR_944078.1:n.1259+1014C=
XM_005268037.4:c.505G=	XP_005268094.1:p.Val169=
XM_011537119.2:c.226G=	XP_011535421.1:p.Val76=
XR_001751018.2:n.700-161C=
XR_001751019.2:n.699+1014C=
XR_001751020.2:n.699+1014C=
XR_001751021.1:n.3148-161C=
XR_001751022.1:n.3147+1014C=
XR_001751023.1:n.3280+1014C=
XR_001751024.2:n.700-161C=
XR_944075.3:n.1324-161C=
NM_000369.4:c.505G=	NP_000360.2:p.Val169=
NM_001018036.3:c.505G=	NP_001018046.1:p.Val169=
NM_001142626.3:c.505G=	NP_001136098.1:p.Val169=
NM_000369.5:c.505G= MANE Select	NP_000360.2:p.Val169=