Canonical Allele Identifier: CA2843040502

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81144551T>G , CM000676.2:g.81144551T>G	GRCh38
NC_000014.8:g.81610895T>G , CM000676.1:g.81610895T>G	GRCh37
NC_000014.7:g.80680648T>G	NCBI36
NG_009206.1:g.194027T>G , LRG_523:g.194027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.*198T>G MANE Select	ENSP00000298171.2:n.*198T>G
ENST00000637447.1:c.1396T>G
ENST00000298171.6:c.*198T>G	ENSP00000298171.2:n.*198T>G
ENST00000541158.6:c.*198T>G	ENSP00000441235.2:n.*198T>G
NM_000369.2:c.*198T>G , LRG_523t1:c.*198T>G	NP_000360.2:n.*198T>G
XM_005268037.3:c.*198T>G	XP_005268094.1:n.*198T>G
XM_011537119.1:c.*198T>G	XP_011535421.1:n.*198T>G
XR_245790.3:n.2086+20642A>C
XR_429385.2:n.853+20642A>C
XR_429386.2:n.854+20642A>C
XR_944075.1:n.865+20642A>C
XR_944076.1:n.861+20642A>C
XR_944077.1:n.865+20642A>C
XR_944078.1:n.865+20642A>C
XR_944079.1:n.855+20642A>C
XM_005268037.4:c.*198T>G	XP_005268094.1:n.*198T>G
XM_011537119.2:c.*198T>G	XP_011535421.1:n.*198T>G
XR_001751021.1:n.2753+20642A>C
XR_001751022.1:n.2753+20642A>C
XR_001751023.1:n.2753+20642A>C
XR_944075.3:n.929+20642A>C
NM_000369.4:c.*198T>G	NP_000360.2:n.*198T>G
NM_000369.5:c.*198T>G MANE Select	NP_000360.2:n.*198T>G