Canonical Allele Identifier: CA263957006
Gene: TSHR HGNC NCBI

Linked Data

dbSNP Id: rs773942819

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.81092463G>A , CM000676.2:g.81092463G>A GRCh38
NC_000014.8:g.81558807G>A , CM000676.1:g.81558807G>A GRCh37
NC_000014.7:g.80628560G>A NCBI36
NG_009206.1:g.141939G>A , LRG_523:g.141939G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298171.7:c.468-68G>A MANE Select ENSP00000298171.2:n.468-68G>A
ENST00000636454.1:n.386-68G>A
ENST00000298171.6:c.468-68G>A ENSP00000298171.2:n.468-68G>A
ENST00000342443.10:c.468-68G>A ENSP00000340113.6:n.468-68G>A
ENST00000541158.6:c.468-68G>A ENSP00000441235.2:n.468-68G>A
ENST00000554263.5:c.468-68G>A ENSP00000451202.1:n.468-68G>A
ENST00000554435.1:c.468-68G>A ENSP00000450549.1:n.468-68G>A
NM_000369.2:c.468-68G>A , LRG_523t1:c.468-68G>A NP_000360.2:n.468-68G>A
NM_001018036.2:c.468-68G>A NP_001018046.1:n.468-68G>A
NM_001142626.2:c.468-68G>A NP_001136098.1:n.468-68G>A
XM_005268037.3:c.468-68G>A XP_005268094.1:n.468-68G>A
XM_005268039.1:c.468-68G>A XP_005268096.1:n.468-68G>A
XM_006720245.1:c.468-68G>A XP_006720308.1:n.468-68G>A
XM_011537119.1:c.189-68G>A XP_011535421.1:n.189-68G>A
XR_245790.3:n.2480+1119C>T
XR_944075.1:n.1260-56C>T
XR_944076.1:n.1255+1119C>T
XR_944077.1:n.1259+1119C>T
XR_944078.1:n.1259+1119C>T
XM_005268037.4:c.468-68G>A XP_005268094.1:n.468-68G>A
XM_011537119.2:c.189-68G>A XP_011535421.1:n.189-68G>A
XR_001751018.2:n.700-56C>T
XR_001751019.2:n.699+1119C>T
XR_001751020.2:n.699+1119C>T
XR_001751021.1:n.3148-56C>T
XR_001751022.1:n.3147+1119C>T
XR_001751023.1:n.3280+1119C>T
XR_001751024.2:n.700-56C>T
XR_944075.3:n.1324-56C>T
NM_000369.4:c.468-68G>A NP_000360.2:n.468-68G>A
NM_001018036.3:c.468-68G>A NP_001018046.1:n.468-68G>A
NM_001142626.3:c.468-68G>A NP_001136098.1:n.468-68G>A
NM_000369.5:c.468-68G>A MANE Select NP_000360.2:n.468-68G>A