Canonical Allele Identifier: CA2625935849

Gene: TSHR

Linked Data

• gnomAD v4: 14-81144522-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81144524dup , CM000676.2:g.81144524dup	GRCh38
NC_000014.8:g.81610868dup , CM000676.1:g.81610868dup	GRCh37
NC_000014.7:g.80680621dup	NCBI36
NG_009206.1:g.194000dup , LRG_523:g.194000dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000298171.7:c.*171dup MANE Select	ENSP00000298171.2:n.*171dup
ENST00000637447.1:c.1369dup
ENST00000298171.6:c.*171dup	ENSP00000298171.2:n.*171dup
ENST00000541158.6:c.*171dup	ENSP00000441235.2:n.*171dup
NM_000369.2:c.*171dup , LRG_523t1:c.*171dup	NP_000360.2:n.*171dup
XM_005268037.3:c.*171dup	XP_005268094.1:n.*171dup
XM_011537119.1:c.*171dup	XP_011535421.1:n.*171dup
XR_245790.3:n.2086+20670dup
XR_429385.2:n.853+20670dup
XR_429386.2:n.854+20670dup
XR_944075.1:n.865+20670dup
XR_944076.1:n.861+20670dup
XR_944077.1:n.865+20670dup
XR_944078.1:n.865+20670dup
XR_944079.1:n.855+20670dup
XM_005268037.4:c.*171dup	XP_005268094.1:n.*171dup
XM_011537119.2:c.*171dup	XP_011535421.1:n.*171dup
XR_001751021.1:n.2753+20670dup
XR_001751022.1:n.2753+20670dup
XR_001751023.1:n.2753+20670dup
XR_944075.3:n.929+20670dup
NM_000369.4:c.*171dup	NP_000360.2:n.*171dup
NM_000369.5:c.*171dup MANE Select	NP_000360.2:n.*171dup