Canonical Allele Identifier: CA2150074801

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81143174C= , CM000676.2:g.81143174C=	GRCh38
NC_000014.8:g.81609518C= , CM000676.1:g.81609518C=	GRCh37
NC_000014.7:g.80679271C=	NCBI36
NG_009206.1:g.192650C= , LRG_523:g.192650C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.1116C= MANE Select	ENSP00000298171.2:p.Asn372=
ENST00000636454.1:n.1034C=
ENST00000637447.1:c.19C=
ENST00000298171.6:c.1116C=	ENSP00000298171.2:p.Asn372=
ENST00000541158.6:c.1116C=	ENSP00000441235.2:p.Asn372=
NM_000369.2:c.1116C= , LRG_523t1:c.1116C=	NP_000360.2:p.Asn372=
XM_005268037.3:c.1116C=	XP_005268094.1:p.Asn372=
XM_011537119.1:c.837C=	XP_011535421.1:p.Asn279=
XR_245790.3:n.2086+22019G=
XR_429385.2:n.853+22019G=
XR_429386.2:n.854+22019G=
XR_944075.1:n.865+22019G=
XR_944076.1:n.861+22019G=
XR_944077.1:n.865+22019G=
XR_944078.1:n.865+22019G=
XR_944079.1:n.855+22019G=
XM_005268037.4:c.1116C=	XP_005268094.1:p.Asn372=
XM_011537119.2:c.837C=	XP_011535421.1:p.Asn279=
XR_001751021.1:n.2753+22019G=
XR_001751022.1:n.2753+22019G=
XR_001751023.1:n.2753+22019G=
XR_944075.3:n.929+22019G=
NM_000369.4:c.1116C=	NP_000360.2:p.Asn372=
NM_000369.5:c.1116C= MANE Select	NP_000360.2:p.Asn372=