Canonical Allele Identifier: CA2150076390

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81144149_81144150delinsCA , CM000676.2:g.81144149_81144150delinsCA	GRCh38
NC_000014.8:g.81610493_81610494delinsCA , CM000676.1:g.81610493_81610494delinsCA	GRCh37
NC_000014.7:g.80680246_80680247delinsCA	NCBI36
NG_009206.1:g.193625_193626delinsCA , LRG_523:g.193625_193626delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.2091_2092delinsCA MANE Select	ENSP00000298171.2:p.Gly697=
ENST00000637447.1:c.994_995delinsCA
ENST00000298171.6:c.2091_2092delinsCA	ENSP00000298171.2:p.Gly697=
ENST00000541158.6:c.2091_2092delinsCA	ENSP00000441235.2:p.Gly697=
NM_000369.2:c.2091_2092delinsCA , LRG_523t1:c.2091_2092delinsCA	NP_000360.2:p.Gly697=
XM_005268037.3:c.2091_2092delinsCA	XP_005268094.1:p.Gly697=
XM_011537119.1:c.1812_1813delinsCA	XP_011535421.1:p.Gly604=
XR_245790.3:n.2086+21043_2086+21044delinsTG
XR_429385.2:n.853+21043_853+21044delinsTG
XR_429386.2:n.854+21043_854+21044delinsTG
XR_944075.1:n.865+21043_865+21044delinsTG
XR_944076.1:n.861+21043_861+21044delinsTG
XR_944077.1:n.865+21043_865+21044delinsTG
XR_944078.1:n.865+21043_865+21044delinsTG
XR_944079.1:n.855+21043_855+21044delinsTG
XM_005268037.4:c.2091_2092delinsCA	XP_005268094.1:p.Gly697=
XM_011537119.2:c.1812_1813delinsCA	XP_011535421.1:p.Gly604=
XR_001751021.1:n.2753+21043_2753+21044delinsTG
XR_001751022.1:n.2753+21043_2753+21044delinsTG
XR_001751023.1:n.2753+21043_2753+21044delinsTG
XR_944075.3:n.929+21043_929+21044delinsTG
NM_000369.4:c.2091_2092delinsCA	NP_000360.2:p.Gly697=
NM_000369.5:c.2091_2092delinsCA MANE Select	NP_000360.2:p.Gly697=