Canonical Allele Identifier: CA390727667

Gene: TSHR

Linked Data

• MyVariant Identifiers: chr14:g.81609738C>A (hg19) ; chr14:g.81143394C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81143394C>A , CM000676.2:g.81143394C>A	GRCh38
NC_000014.8:g.81609738C>A , CM000676.1:g.81609738C>A	GRCh37
NC_000014.7:g.80679491C>A	NCBI36
NG_009206.1:g.192870C>A , LRG_523:g.192870C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298171.7:c.1336C>A MANE Select	ENSP00000298171.2:p.Leu446Met
ENST00000636454.1:n.1254C>A
ENST00000637447.1:c.239C>A
ENST00000298171.6:c.1336C>A	ENSP00000298171.2:p.Leu446Met
ENST00000541158.6:c.1336C>A	ENSP00000441235.2:p.Leu446Met
NM_000369.2:c.1336C>A , LRG_523t1:c.1336C>A	NP_000360.2:p.Leu446Met
XM_005268037.3:c.1336C>A	XP_005268094.1:p.Leu446Met
XM_011537119.1:c.1057C>A	XP_011535421.1:p.Leu353Met
XR_245790.3:n.2086+21799G>T
XR_429385.2:n.853+21799G>T
XR_429386.2:n.854+21799G>T
XR_944075.1:n.865+21799G>T
XR_944076.1:n.861+21799G>T
XR_944077.1:n.865+21799G>T
XR_944078.1:n.865+21799G>T
XR_944079.1:n.855+21799G>T
XM_005268037.4:c.1336C>A	XP_005268094.1:p.Leu446Met
XM_011537119.2:c.1057C>A	XP_011535421.1:p.Leu353Met
XR_001751021.1:n.2753+21799G>T
XR_001751022.1:n.2753+21799G>T
XR_001751023.1:n.2753+21799G>T
XR_944075.3:n.929+21799G>T
NM_000369.4:c.1336C>A	NP_000360.2:p.Leu446Met
NM_000369.5:c.1336C>A MANE Select	NP_000360.2:p.Leu446Met