Canonical Allele Identifier: CA2150076980

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81144518G= , CM000676.2:g.81144518G=	GRCh38
NC_000014.8:g.81610862G= , CM000676.1:g.81610862G=	GRCh37
NC_000014.7:g.80680615G=	NCBI36
NG_009206.1:g.193994G= , LRG_523:g.193994G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298171.7:c.*165G= MANE Select	ENSP00000298171.2:n.*165G=
ENST00000637447.1:c.1363G=
ENST00000298171.6:c.*165G=	ENSP00000298171.2:n.*165G=
ENST00000541158.6:c.*165G=	ENSP00000441235.2:n.*165G=
NM_000369.2:c.*165G= , LRG_523t1:c.*165G=	NP_000360.2:n.*165G=
XM_005268037.3:c.*165G=	XP_005268094.1:n.*165G=
XM_011537119.1:c.*165G=	XP_011535421.1:n.*165G=
XR_245790.3:n.2086+20675C=
XR_429385.2:n.853+20675C=
XR_429386.2:n.854+20675C=
XR_944075.1:n.865+20675C=
XR_944076.1:n.861+20675C=
XR_944077.1:n.865+20675C=
XR_944078.1:n.865+20675C=
XR_944079.1:n.855+20675C=
XM_005268037.4:c.*165G=	XP_005268094.1:n.*165G=
XM_011537119.2:c.*165G=	XP_011535421.1:n.*165G=
XR_001751021.1:n.2753+20675C=
XR_001751022.1:n.2753+20675C=
XR_001751023.1:n.2753+20675C=
XR_944075.3:n.929+20675C=
NM_000369.4:c.*165G=	NP_000360.2:n.*165G=
NM_000369.5:c.*165G= MANE Select	NP_000360.2:n.*165G=