Canonical Allele Identifier: CA487512935

Gene: TSHR

Linked Data

• MyVariant Identifiers: chr14:g.81610601C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81144257C>T , CM000676.2:g.81144257C>T	GRCh38
NC_000014.8:g.81610601C>T , CM000676.1:g.81610601C>T	GRCh37
NC_000014.7:g.80680354C>T	NCBI36
NG_009206.1:g.193733C>T , LRG_523:g.193733C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.2199C>T MANE Select	ENSP00000298171.2:p.His733=
ENST00000637447.1:c.1102C>T
ENST00000298171.6:c.2199C>T	ENSP00000298171.2:p.His733=
ENST00000541158.6:c.2199C>T	ENSP00000441235.2:p.His733=
NM_000369.2:c.2199C>T , LRG_523t1:c.2199C>T	NP_000360.2:p.His733=
XM_005268037.3:c.2199C>T	XP_005268094.1:p.His733=
XM_011537119.1:c.1920C>T	XP_011535421.1:p.His640=
XR_245790.3:n.2086+20936G>A
XR_429385.2:n.853+20936G>A
XR_429386.2:n.854+20936G>A
XR_944075.1:n.865+20936G>A
XR_944076.1:n.861+20936G>A
XR_944077.1:n.865+20936G>A
XR_944078.1:n.865+20936G>A
XR_944079.1:n.855+20936G>A
XM_005268037.4:c.2199C>T	XP_005268094.1:p.His733=
XM_011537119.2:c.1920C>T	XP_011535421.1:p.His640=
XR_001751021.1:n.2753+20936G>A
XR_001751022.1:n.2753+20936G>A
XR_001751023.1:n.2753+20936G>A
XR_944075.3:n.929+20936G>A
NM_000369.4:c.2199C>T	NP_000360.2:p.His733=
NM_000369.5:c.2199C>T MANE Select	NP_000360.2:p.His733=