Canonical Allele Identifier: CA2150096611

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81128036C= , CM000676.2:g.81128036C=	GRCh38
NC_000014.8:g.81594380C= , CM000676.1:g.81594380C=	GRCh37
NC_000014.7:g.80664133C=	NCBI36
NG_009206.1:g.177512C= , LRG_523:g.177512C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.693-11643C= MANE Select	ENSP00000298171.2:n.693-11643C=
ENST00000636454.1:n.611-11643C=
ENST00000298171.6:c.693-11643C=	ENSP00000298171.2:n.693-11643C=
ENST00000541158.6:c.693-11643C=	ENSP00000441235.2:n.693-11643C=
NM_000369.2:c.693-11643C= , LRG_523t1:c.693-11643C=	NP_000360.2:n.693-11643C=
XM_005268037.3:c.693-11643C=	XP_005268094.1:n.693-11643C=
XM_011537119.1:c.414-11643C=	XP_011535421.1:n.414-11643C=
XR_245790.3:n.2087-28510G=
XR_429385.2:n.854-20856G=
XR_429386.2:n.855-20898G=
XR_944075.1:n.866-28510G=
XR_944076.1:n.862-28510G=
XR_944077.1:n.866-28510G=
XR_944078.1:n.866-28510G=
XR_944079.1:n.856-20856G=
XM_005268037.4:c.693-11643C=	XP_005268094.1:n.693-11643C=
XM_011537119.2:c.414-11643C=	XP_011535421.1:n.414-11643C=
XR_001751021.1:n.2754-28510G=
XR_001751022.1:n.2754-28510G=
XR_001751023.1:n.2754-28510G=
XR_944075.3:n.930-28510G=
NM_000369.4:c.693-11643C=	NP_000360.2:n.693-11643C=
NM_000369.5:c.693-11643C= MANE Select	NP_000360.2:n.693-11643C=