Canonical Allele Identifier: CA2150070603

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81092566C= , CM000676.2:g.81092566C=	GRCh38
NC_000014.8:g.81558910C= , CM000676.1:g.81558910C=	GRCh37
NC_000014.7:g.80628663C=	NCBI36
NG_009206.1:g.142042C= , LRG_523:g.142042C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.503C= MANE Select	ENSP00000298171.2:p.Pro168=
ENST00000636454.1:n.421C=
ENST00000298171.6:c.503C=	ENSP00000298171.2:p.Pro168=
ENST00000342443.10:c.503C=	ENSP00000340113.6:p.Pro168=
ENST00000541158.6:c.503C=	ENSP00000441235.2:p.Pro168=
ENST00000554263.5:c.503C=	ENSP00000451202.1:p.Pro168=
ENST00000554435.1:c.503C=	ENSP00000450549.1:p.Pro168=
NM_000369.2:c.503C= , LRG_523t1:c.503C=	NP_000360.2:p.Pro168=
NM_001018036.2:c.503C=	NP_001018046.1:p.Pro168=
NM_001142626.2:c.503C=	NP_001136098.1:p.Pro168=
XM_005268037.3:c.503C=	XP_005268094.1:p.Pro168=
XM_005268039.1:c.503C=	XP_005268096.1:p.Pro168=
XM_006720245.1:c.503C=	XP_006720308.1:p.Pro168=
XM_011537119.1:c.224C=	XP_011535421.1:p.Pro75=
XR_245790.3:n.2480+1016G=
XR_944075.1:n.1260-159G=
XR_944076.1:n.1255+1016G=
XR_944077.1:n.1259+1016G=
XR_944078.1:n.1259+1016G=
XM_005268037.4:c.503C=	XP_005268094.1:p.Pro168=
XM_011537119.2:c.224C=	XP_011535421.1:p.Pro75=
XR_001751018.2:n.700-159G=
XR_001751019.2:n.699+1016G=
XR_001751020.2:n.699+1016G=
XR_001751021.1:n.3148-159G=
XR_001751022.1:n.3147+1016G=
XR_001751023.1:n.3280+1016G=
XR_001751024.2:n.700-159G=
XR_944075.3:n.1324-159G=
NM_000369.4:c.503C=	NP_000360.2:p.Pro168=
NM_001018036.3:c.503C=	NP_001018046.1:p.Pro168=
NM_001142626.3:c.503C=	NP_001136098.1:p.Pro168=
NM_000369.5:c.503C= MANE Select	NP_000360.2:p.Pro168=