Canonical Allele Identifier: CA2688233063

Gene: TRHR

Linked Data

• gnomAD v4: 8-109087609-C-CTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087611_109087613dup , CM000670.2:g.109087611_109087613dup	GRCh38
NC_000008.10:g.110099840_110099842dup , CM000670.1:g.110099840_110099842dup	GRCh37
NC_000008.9:g.110169016_110169018dup	NCBI36
NG_017161.1:g.5165_5167dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.99_101dup MANE Select	ENSP00000430711.2:p.Ile34_Ile35insIle
ENST00000311762.2:c.99_101dup	ENSP00000309818.2:p.Ile34_Ile35insIle
ENST00000518632.1:c.99_101dup	ENSP00000430711.1:p.Ile34_Ile35insIle
NM_003301.5:c.99_101dup	NP_003292.1:p.Ile34_Ile35insIle
XM_011517263.1:c.99_101dup	XP_011515565.1:p.Ile34_Ile35insIle
XM_011517263.2:c.99_101dup	XP_011515565.1:p.Ile34_Ile35insIle
NM_003301.7:c.99_101dup MANE Select	NP_003292.1:p.Ile34_Ile35insIle