Canonical Allele Identifier: CA8539296
Gene: THRA HGNC NCBI

Linked Data

dbSNP Id: rs781699391

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40089323T>C , CM000679.2:g.40089323T>C GRCh38
NC_000017.10:g.38245576T>C , CM000679.1:g.38245576T>C GRCh37
NC_000017.9:g.35499102T>C NCBI36
NG_023345.1:g.32131T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000450525.7:c.1100T>C MANE Select ENSP00000395641.3:p.Leu367Pro
ENST00000264637.8:c.1100T>C ENSP00000264637.4:p.Leu367Pro
ENST00000394121.8:c.1100T>C ENSP00000377679.4:p.Leu367Pro
ENST00000450525.6:c.1100T>C ENSP00000395641.2:p.Leu367Pro
ENST00000546243.5:c.1100T>C ENSP00000443972.1:p.Leu367Pro
ENST00000584985.5:c.1100T>C ENSP00000463466.1:p.Leu367Pro
NM_001190918.1:c.1100T>C NP_001177847.1:p.Leu367Pro
NM_001190919.1:c.1100T>C NP_001177848.1:p.Leu367Pro
NM_003250.5:c.1100T>C NP_003241.2:p.Leu367Pro
NM_199334.3:c.1100T>C NP_955366.1:p.Leu367Pro
NM_001190918.2:c.1100T>C NP_001177847.1:p.Leu367Pro
NM_003250.6:c.1100T>C NP_003241.2:p.Leu367Pro
NM_199334.5:c.1100T>C MANE Select NP_955366.1:p.Leu367Pro
NM_001190919.2:c.1100T>C NP_001177848.1:p.Leu367Pro