Canonical Allele Identifier: CA2150060291

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81068425_81068427delinsTTG , CM000676.2:g.81068425_81068427delinsTTG	GRCh38
NC_000014.8:g.81534769_81534771delinsTTG , CM000676.1:g.81534769_81534771delinsTTG	GRCh37
NC_000014.7:g.80604522_80604524delinsTTG	NCBI36
NG_009206.1:g.117901_117903delinsTTG , LRG_523:g.117901_117903delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.317+97_317+99delinsTTG MANE Select	ENSP00000298171.2:n.317+97_317+99delinsTTG
ENST00000298171.6:c.317+97_317+99delinsTTG	ENSP00000298171.2:n.317+97_317+99delinsTTG
ENST00000342443.10:c.317+97_317+99delinsTTG	ENSP00000340113.6:n.317+97_317+99delinsTTG
ENST00000541158.6:c.317+97_317+99delinsTTG	ENSP00000441235.2:n.317+97_317+99delinsTTG
ENST00000553763.1:n.514_516delinsTTG
ENST00000554263.5:c.317+97_317+99delinsTTG	ENSP00000451202.1:n.317+97_317+99delinsTTG
ENST00000554435.1:c.317+97_317+99delinsTTG	ENSP00000450549.1:n.317+97_317+99delinsTTG
ENST00000555326.5:c.317+97_317+99delinsTTG	ENSP00000451092.1:n.317+97_317+99delinsTTG
NM_000369.2:c.317+97_317+99delinsTTG , LRG_523t1:c.317+97_317+99delinsTTG	NP_000360.2:n.317+97_317+99delinsTTG
NM_001018036.2:c.317+97_317+99delinsTTG	NP_001018046.1:n.317+97_317+99delinsTTG
NM_001142626.2:c.317+97_317+99delinsTTG	NP_001136098.1:n.317+97_317+99delinsTTG
XM_005268037.3:c.317+97_317+99delinsTTG	XP_005268094.1:n.317+97_317+99delinsTTG
XM_005268039.1:c.317+97_317+99delinsTTG	XP_005268096.1:n.317+97_317+99delinsTTG
XM_006720245.1:c.317+97_317+99delinsTTG	XP_006720308.1:n.317+97_317+99delinsTTG
XM_011537119.1:c.-12+97_-12+99delinsTTG	XP_011535421.1:n.-12+97_-12+99delinsTTG
XR_245790.3:n.3676-14611_3676-14609delinsCAA
XR_944075.1:n.2549-14611_2549-14609delinsCAA
XR_944076.1:n.1442-14611_1442-14609delinsCAA
XR_944077.1:n.2455-14611_2455-14609delinsCAA
XR_944078.1:n.2455-14611_2455-14609delinsCAA
XM_005268037.4:c.317+97_317+99delinsTTG	XP_005268094.1:n.317+97_317+99delinsTTG
XM_011537119.2:c.-12+97_-12+99delinsTTG	XP_011535421.1:n.-12+97_-12+99delinsTTG
XR_001751018.2:n.1989-14611_1989-14609delinsCAA
XR_001751019.2:n.1895-14611_1895-14609delinsCAA
XR_001751020.2:n.886-14611_886-14609delinsCAA
XR_001751021.1:n.4437-14611_4437-14609delinsCAA
XR_001751022.1:n.3334-14611_3334-14609delinsCAA
XR_001751023.1:n.4476-14611_4476-14609delinsCAA
XR_001751024.2:n.1989-14611_1989-14609delinsCAA
XR_944075.3:n.2613-14611_2613-14609delinsCAA
NM_000369.4:c.317+97_317+99delinsTTG	NP_000360.2:n.317+97_317+99delinsTTG
NM_001018036.3:c.317+97_317+99delinsTTG	NP_001018046.1:n.317+97_317+99delinsTTG
NM_001142626.3:c.317+97_317+99delinsTTG	NP_001136098.1:n.317+97_317+99delinsTTG
NM_000369.5:c.317+97_317+99delinsTTG MANE Select	NP_000360.2:n.317+97_317+99delinsTTG