Canonical Allele Identifier: CA487512621

Gene: TSHR

Linked Data

• MyVariant Identifiers: chr14:g.81609899C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81143555C>T , CM000676.2:g.81143555C>T	GRCh38
NC_000014.8:g.81609899C>T , CM000676.1:g.81609899C>T	GRCh37
NC_000014.7:g.80679652C>T	NCBI36
NG_009206.1:g.193031C>T , LRG_523:g.193031C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.1497C>T MANE Select	ENSP00000298171.2:p.Phe499=
ENST00000636454.1:n.1415C>T
ENST00000637447.1:c.400C>T
ENST00000298171.6:c.1497C>T	ENSP00000298171.2:p.Phe499=
ENST00000541158.6:c.1497C>T	ENSP00000441235.2:p.Phe499=
NM_000369.2:c.1497C>T , LRG_523t1:c.1497C>T	NP_000360.2:p.Phe499=
XM_005268037.3:c.1497C>T	XP_005268094.1:p.Phe499=
XM_011537119.1:c.1218C>T	XP_011535421.1:p.Phe406=
XR_245790.3:n.2086+21638G>A
XR_429385.2:n.853+21638G>A
XR_429386.2:n.854+21638G>A
XR_944075.1:n.865+21638G>A
XR_944076.1:n.861+21638G>A
XR_944077.1:n.865+21638G>A
XR_944078.1:n.865+21638G>A
XR_944079.1:n.855+21638G>A
XM_005268037.4:c.1497C>T	XP_005268094.1:p.Phe499=
XM_011537119.2:c.1218C>T	XP_011535421.1:p.Phe406=
XR_001751021.1:n.2753+21638G>A
XR_001751022.1:n.2753+21638G>A
XR_001751023.1:n.2753+21638G>A
XR_944075.3:n.929+21638G>A
NM_000369.4:c.1497C>T	NP_000360.2:p.Phe499=
NM_000369.5:c.1497C>T MANE Select	NP_000360.2:p.Phe499=