Canonical Allele Identifier: CA8539297
Gene: THRA HGNC NCBI

Linked Data

dbSNP Id: rs577276332

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40089328A>T , CM000679.2:g.40089328A>T GRCh38
NC_000017.10:g.38245581A>T , CM000679.1:g.38245581A>T GRCh37
NC_000017.9:g.35499107A>T NCBI36
NG_023345.1:g.32136A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000450525.7:c.1105A>T MANE Select ENSP00000395641.3:p.Met369Leu
ENST00000264637.8:c.1105A>T ENSP00000264637.4:p.Met369Leu
ENST00000394121.8:c.1105A>T ENSP00000377679.4:p.Met369Leu
ENST00000450525.6:c.1105A>T ENSP00000395641.2:p.Met369Leu
ENST00000546243.5:c.1105A>T ENSP00000443972.1:p.Met369Leu
ENST00000584985.5:c.1105A>T ENSP00000463466.1:p.Met369Leu
NM_001190918.1:c.1105A>T NP_001177847.1:p.Met369Leu
NM_001190919.1:c.1105A>T NP_001177848.1:p.Met369Leu
NM_003250.5:c.1105A>T NP_003241.2:p.Met369Leu
NM_199334.3:c.1105A>T NP_955366.1:p.Met369Leu
NM_001190918.2:c.1105A>T NP_001177847.1:p.Met369Leu
NM_003250.6:c.1105A>T NP_003241.2:p.Met369Leu
NM_199334.5:c.1105A>T MANE Select NP_955366.1:p.Met369Leu
NM_001190919.2:c.1105A>T NP_001177848.1:p.Met369Leu