Canonical Allele Identifier: CA2150074469

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81142910T= , CM000676.2:g.81142910T=	GRCh38
NC_000014.8:g.81609254T= , CM000676.1:g.81609254T=	GRCh37
NC_000014.7:g.80679007T=	NCBI36
NG_009206.1:g.192386T= , LRG_523:g.192386T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.882-30T= MANE Select	ENSP00000298171.2:n.882-30T=
ENST00000636454.1:n.800-30T=
ENST00000298171.6:c.882-30T=	ENSP00000298171.2:n.882-30T=
ENST00000541158.6:c.882-30T=	ENSP00000441235.2:n.882-30T=
NM_000369.2:c.882-30T= , LRG_523t1:c.882-30T=	NP_000360.2:n.882-30T=
XM_005268037.3:c.882-30T=	XP_005268094.1:n.882-30T=
XM_011537119.1:c.603-30T=	XP_011535421.1:n.603-30T=
XR_245790.3:n.2086+22283A=
XR_429385.2:n.853+22283A=
XR_429386.2:n.854+22283A=
XR_944075.1:n.865+22283A=
XR_944076.1:n.861+22283A=
XR_944077.1:n.865+22283A=
XR_944078.1:n.865+22283A=
XR_944079.1:n.855+22283A=
XM_005268037.4:c.882-30T=	XP_005268094.1:n.882-30T=
XM_011537119.2:c.603-30T=	XP_011535421.1:n.603-30T=
XR_001751021.1:n.2753+22283A=
XR_001751022.1:n.2753+22283A=
XR_001751023.1:n.2753+22283A=
XR_944075.3:n.929+22283A=
NM_000369.4:c.882-30T=	NP_000360.2:n.882-30T=
NM_000369.5:c.882-30T= MANE Select	NP_000360.2:n.882-30T=