Canonical Allele Identifier: CA390728513

Gene: TSHR

Linked Data

• MyVariant Identifiers: chr14:g.81610137G>T (hg19) ; chr14:g.81143793G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81143793G>T , CM000676.2:g.81143793G>T	GRCh38
NC_000014.8:g.81610137G>T , CM000676.1:g.81610137G>T	GRCh37
NC_000014.7:g.80679890G>T	NCBI36
NG_009206.1:g.193269G>T , LRG_523:g.193269G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298171.7:c.1735G>T MANE Select	ENSP00000298171.2:p.Ala579Ser
ENST00000637447.1:c.638G>T
ENST00000298171.6:c.1735G>T	ENSP00000298171.2:p.Ala579Ser
ENST00000541158.6:c.1735G>T	ENSP00000441235.2:p.Ala579Ser
NM_000369.2:c.1735G>T , LRG_523t1:c.1735G>T	NP_000360.2:p.Ala579Ser
XM_005268037.3:c.1735G>T	XP_005268094.1:p.Ala579Ser
XM_011537119.1:c.1456G>T	XP_011535421.1:p.Ala486Ser
XR_245790.3:n.2086+21400C>A
XR_429385.2:n.853+21400C>A
XR_429386.2:n.854+21400C>A
XR_944075.1:n.865+21400C>A
XR_944076.1:n.861+21400C>A
XR_944077.1:n.865+21400C>A
XR_944078.1:n.865+21400C>A
XR_944079.1:n.855+21400C>A
XM_005268037.4:c.1735G>T	XP_005268094.1:p.Ala579Ser
XM_011537119.2:c.1456G>T	XP_011535421.1:p.Ala486Ser
XR_001751021.1:n.2753+21400C>A
XR_001751022.1:n.2753+21400C>A
XR_001751023.1:n.2753+21400C>A
XR_944075.3:n.929+21400C>A
NM_000369.4:c.1735G>T	NP_000360.2:p.Ala579Ser
NM_000369.5:c.1735G>T MANE Select	NP_000360.2:p.Ala579Ser