Canonical Allele Identifier: CA399274760

Gene: THRA

Linked Data

• ClinVar Variation Id: 522121
• ClinVar RCV Id: RCV000623448 ; RCV002305517 ; RCV003129944
• dbSNP Id: rs1555545033
• MyVariant Identifiers: chr17:g.38244559C>T (hg19) ; chr17:g.40088306C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40088306C>T , CM000679.2:g.40088306C>T	GRCh38
NC_000017.10:g.38244559C>T , CM000679.1:g.38244559C>T	GRCh37
NC_000017.9:g.35498085C>T	NCBI36
NG_023345.1:g.31114C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450525.7:c.788C>T MANE Select	ENSP00000395641.3:p.Ala263Val
ENST00000264637.8:c.788C>T	ENSP00000264637.4:p.Ala263Val
ENST00000394121.8:c.788C>T	ENSP00000377679.4:p.Ala263Val
ENST00000450525.6:c.788C>T	ENSP00000395641.2:p.Ala263Val
ENST00000546243.5:c.788C>T	ENSP00000443972.1:p.Ala263Val
ENST00000584985.5:c.788C>T	ENSP00000463466.1:p.Ala263Val
NM_001190918.1:c.788C>T	NP_001177847.1:p.Ala263Val
NM_001190919.1:c.788C>T	NP_001177848.1:p.Ala263Val
NM_003250.5:c.788C>T	NP_003241.2:p.Ala263Val
NM_199334.3:c.788C>T	NP_955366.1:p.Ala263Val
NM_001190918.2:c.788C>T	NP_001177847.1:p.Ala263Val
NM_003250.6:c.788C>T	NP_003241.2:p.Ala263Val
NM_199334.5:c.788C>T MANE Select	NP_955366.1:p.Ala263Val
NM_001190919.2:c.788C>T	NP_001177848.1:p.Ala263Val