Canonical Allele Identifier: CA709035876

Gene: TSHR

Linked Data

• dbSNP Id: rs1192611749
• MyVariant Identifiers: chr14:g.81534555_81534556del (hg19) ; chr14:g.81068211_81068212del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81068211_81068212del , CM000676.2:g.81068211_81068212del	GRCh38
NC_000014.8:g.81534555_81534556del , CM000676.1:g.81534555_81534556del	GRCh37
NC_000014.7:g.80604308_80604309del	NCBI36
NG_009206.1:g.117687_117688del , LRG_523:g.117687_117688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.243-43_243-42del MANE Select	ENSP00000298171.2:n.243-43_243-42del
ENST00000298171.6:c.243-43_243-42del	ENSP00000298171.2:n.243-43_243-42del
ENST00000342443.10:c.243-43_243-42del	ENSP00000340113.6:n.243-43_243-42del
ENST00000541158.6:c.243-43_243-42del	ENSP00000441235.2:n.243-43_243-42del
ENST00000553763.1:n.343-43_343-42del
ENST00000554263.5:c.243-43_243-42del	ENSP00000451202.1:n.243-43_243-42del
ENST00000554435.1:c.243-43_243-42del	ENSP00000450549.1:n.243-43_243-42del
ENST00000555326.5:c.243-43_243-42del	ENSP00000451092.1:n.243-43_243-42del
NM_000369.2:c.243-43_243-42del , LRG_523t1:c.243-43_243-42del	NP_000360.2:n.243-43_243-42del
NM_001018036.2:c.243-43_243-42del	NP_001018046.1:n.243-43_243-42del
NM_001142626.2:c.243-43_243-42del	NP_001136098.1:n.243-43_243-42del
XM_005268037.3:c.243-43_243-42del	XP_005268094.1:n.243-43_243-42del
XM_005268039.1:c.243-43_243-42del	XP_005268096.1:n.243-43_243-42del
XM_006720245.1:c.243-43_243-42del	XP_006720308.1:n.243-43_243-42del
XM_011537119.1:c.-86-43_-86-42del	XP_011535421.1:n.-86-43_-86-42del
XR_245790.3:n.3676-14396_3676-14395del
XR_944075.1:n.2549-14396_2549-14395del
XR_944076.1:n.1442-14396_1442-14395del
XR_944077.1:n.2455-14396_2455-14395del
XR_944078.1:n.2455-14396_2455-14395del
XM_005268037.4:c.243-43_243-42del	XP_005268094.1:n.243-43_243-42del
XM_011537119.2:c.-86-43_-86-42del	XP_011535421.1:n.-86-43_-86-42del
XR_001751018.2:n.1989-14396_1989-14395del
XR_001751019.2:n.1895-14396_1895-14395del
XR_001751020.2:n.886-14396_886-14395del
XR_001751021.1:n.4437-14396_4437-14395del
XR_001751022.1:n.3334-14396_3334-14395del
XR_001751023.1:n.4476-14396_4476-14395del
XR_001751024.2:n.1989-14396_1989-14395del
XR_944075.3:n.2613-14396_2613-14395del
NM_000369.4:c.243-43_243-42del	NP_000360.2:n.243-43_243-42del
NM_001018036.3:c.243-43_243-42del	NP_001018046.1:n.243-43_243-42del
NM_001142626.3:c.243-43_243-42del	NP_001136098.1:n.243-43_243-42del
NM_000369.5:c.243-43_243-42del MANE Select	NP_000360.2:n.243-43_243-42del