Canonical Allele Identifier: CA2150075384

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81143536G= , CM000676.2:g.81143536G=	GRCh38
NC_000014.8:g.81609880G= , CM000676.1:g.81609880G=	GRCh37
NC_000014.7:g.80679633G=	NCBI36
NG_009206.1:g.193012G= , LRG_523:g.193012G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.1478G= MANE Select	ENSP00000298171.2:p.Gly493=
ENST00000636454.1:n.1396G=
ENST00000637447.1:c.381G=
ENST00000298171.6:c.1478G=	ENSP00000298171.2:p.Gly493=
ENST00000541158.6:c.1478G=	ENSP00000441235.2:p.Gly493=
NM_000369.2:c.1478G= , LRG_523t1:c.1478G=	NP_000360.2:p.Gly493=
XM_005268037.3:c.1478G=	XP_005268094.1:p.Gly493=
XM_011537119.1:c.1199G=	XP_011535421.1:p.Gly400=
XR_245790.3:n.2086+21657C=
XR_429385.2:n.853+21657C=
XR_429386.2:n.854+21657C=
XR_944075.1:n.865+21657C=
XR_944076.1:n.861+21657C=
XR_944077.1:n.865+21657C=
XR_944078.1:n.865+21657C=
XR_944079.1:n.855+21657C=
XM_005268037.4:c.1478G=	XP_005268094.1:p.Gly493=
XM_011537119.2:c.1199G=	XP_011535421.1:p.Gly400=
XR_001751021.1:n.2753+21657C=
XR_001751022.1:n.2753+21657C=
XR_001751023.1:n.2753+21657C=
XR_944075.3:n.929+21657C=
NM_000369.4:c.1478G=	NP_000360.2:p.Gly493=
NM_000369.5:c.1478G= MANE Select	NP_000360.2:p.Gly493=