Canonical Allele Identifier: CA2150076978

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81144517A= , CM000676.2:g.81144517A=	GRCh38
NC_000014.8:g.81610861A= , CM000676.1:g.81610861A=	GRCh37
NC_000014.7:g.80680614A=	NCBI36
NG_009206.1:g.193993A= , LRG_523:g.193993A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.*164A= MANE Select	ENSP00000298171.2:n.*164A=
ENST00000637447.1:c.1362A=
ENST00000298171.6:c.*164A=	ENSP00000298171.2:n.*164A=
ENST00000541158.6:c.*164A=	ENSP00000441235.2:n.*164A=
NM_000369.2:c.*164A= , LRG_523t1:c.*164A=	NP_000360.2:n.*164A=
XM_005268037.3:c.*164A=	XP_005268094.1:n.*164A=
XM_011537119.1:c.*164A=	XP_011535421.1:n.*164A=
XR_245790.3:n.2086+20676T=
XR_429385.2:n.853+20676T=
XR_429386.2:n.854+20676T=
XR_944075.1:n.865+20676T=
XR_944076.1:n.861+20676T=
XR_944077.1:n.865+20676T=
XR_944078.1:n.865+20676T=
XR_944079.1:n.855+20676T=
XM_005268037.4:c.*164A=	XP_005268094.1:n.*164A=
XM_011537119.2:c.*164A=	XP_011535421.1:n.*164A=
XR_001751021.1:n.2753+20676T=
XR_001751022.1:n.2753+20676T=
XR_001751023.1:n.2753+20676T=
XR_944075.3:n.929+20676T=
NM_000369.4:c.*164A=	NP_000360.2:n.*164A=
NM_000369.5:c.*164A= MANE Select	NP_000360.2:n.*164A=