Canonical Allele Identifier: CA487340114
Gene: TSHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.81558929A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.81092585A>T , CM000676.2:g.81092585A>T GRCh38
NC_000014.8:g.81558929A>T , CM000676.1:g.81558929A>T GRCh37
NC_000014.7:g.80628682A>T NCBI36
NG_009206.1:g.142061A>T , LRG_523:g.142061A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298171.7:c.522A>T MANE Select ENSP00000298171.2:p.Gly174=
ENST00000636454.1:n.440A>T
ENST00000298171.6:c.522A>T ENSP00000298171.2:p.Gly174=
ENST00000342443.10:c.522A>T ENSP00000340113.6:p.Gly174=
ENST00000541158.6:c.522A>T ENSP00000441235.2:p.Gly174=
ENST00000554263.5:c.522A>T ENSP00000451202.1:p.Gly174=
ENST00000554435.1:c.522A>T ENSP00000450549.1:p.Gly174=
NM_000369.2:c.522A>T , LRG_523t1:c.522A>T NP_000360.2:p.Gly174=
NM_001018036.2:c.522A>T NP_001018046.1:p.Gly174=
NM_001142626.2:c.522A>T NP_001136098.1:p.Gly174=
XM_005268037.3:c.522A>T XP_005268094.1:p.Gly174=
XM_005268039.1:c.522A>T XP_005268096.1:p.Gly174=
XM_006720245.1:c.522A>T XP_006720308.1:p.Gly174=
XM_011537119.1:c.243A>T XP_011535421.1:p.Gly81=
XR_245790.3:n.2480+997T>A
XR_944075.1:n.1260-178T>A
XR_944076.1:n.1255+997T>A
XR_944077.1:n.1259+997T>A
XR_944078.1:n.1259+997T>A
XM_005268037.4:c.522A>T XP_005268094.1:p.Gly174=
XM_011537119.2:c.243A>T XP_011535421.1:p.Gly81=
XR_001751018.2:n.700-178T>A
XR_001751019.2:n.699+997T>A
XR_001751020.2:n.699+997T>A
XR_001751021.1:n.3148-178T>A
XR_001751022.1:n.3147+997T>A
XR_001751023.1:n.3280+997T>A
XR_001751024.2:n.700-178T>A
XR_944075.3:n.1324-178T>A
NM_000369.4:c.522A>T NP_000360.2:p.Gly174=
NM_001018036.3:c.522A>T NP_001018046.1:p.Gly174=
NM_001142626.3:c.522A>T NP_001136098.1:p.Gly174=
NM_000369.5:c.522A>T MANE Select NP_000360.2:p.Gly174=