Canonical Allele Identifier: CA128759

Gene: THRA

Linked Data

• ClinVar Variation Id: 29913
• ClinVar RCV Id: RCV000022800
• dbSNP Id: rs137853162
• MyVariant Identifiers: chr17:g.38233773G>T (hg19) ; chr17:g.40077520G>T (hg38)
• PubMed: PMID:22168587 ; PMID:25670821

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40077520G>T , CM000679.2:g.40077520G>T	GRCh38
NC_000017.10:g.38233773G>T , CM000679.1:g.38233773G>T	GRCh37
NC_000017.9:g.35487299G>T	NCBI36
NG_023345.1:g.20328G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450525.7:c.134G>T MANE Select	ENSP00000395641.3:p.Ser45Ile
ENST00000264637.8:c.134G>T	ENSP00000264637.4:p.Ser45Ile
ENST00000394121.8:c.134G>T	ENSP00000377679.4:p.Ser45Ile
ENST00000450525.6:c.134G>T	ENSP00000395641.2:p.Ser45Ile
ENST00000546243.5:c.134G>T	ENSP00000443972.1:p.Ser45Ile
ENST00000577486.1:c.134G>T	ENSP00000464414.1:p.Ser45Ile
ENST00000578218.5:c.134G>T	ENSP00000464123.1:p.Ser45Ile
ENST00000584985.5:c.134G>T	ENSP00000463466.1:p.Ser45Ile
ENST00000585047.5:c.134G>T	ENSP00000462955.1:p.Ser45Ile
NM_001190918.1:c.134G>T	NP_001177847.1:p.Ser45Ile
NM_001190919.1:c.134G>T	NP_001177848.1:p.Ser45Ile
NM_003250.5:c.134G>T	NP_003241.2:p.Ser45Ile
NM_199334.3:c.134G>T	NP_955366.1:p.Ser45Ile
NM_001190918.2:c.134G>T	NP_001177847.1:p.Ser45Ile
NM_003250.6:c.134G>T	NP_003241.2:p.Ser45Ile
NM_199334.5:c.134G>T MANE Select	NP_955366.1:p.Ser45Ile
NM_001190919.2:c.134G>T	NP_001177848.1:p.Ser45Ile