Canonical Allele Identifier: CA399278497

Gene: THRA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40089389A>G , CM000679.2:g.40089389A>G	GRCh38
NC_000017.10:g.38245642A>G , CM000679.1:g.38245642A>G	GRCh37
NC_000017.9:g.35499168A>G	NCBI36
NG_023345.1:g.32197A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450525.7:c.1166A>G MANE Select	ENSP00000395641.3:p.Lys389Arg
ENST00000264637.8:c.1110+56A>G	ENSP00000264637.4:n.1110+56A>G
ENST00000394121.8:c.1110+56A>G	ENSP00000377679.4:n.1110+56A>G
ENST00000450525.6:c.1166A>G	ENSP00000395641.2:p.Lys389Arg
ENST00000546243.5:c.1166A>G	ENSP00000443972.1:p.Lys389Arg
ENST00000584985.5:c.1110+56A>G	ENSP00000463466.1:n.1110+56A>G
NM_001190918.1:c.1110+56A>G	NP_001177847.1:n.1110+56A>G
NM_001190919.1:c.1110+56A>G	NP_001177848.1:n.1110+56A>G
NM_003250.5:c.1110+56A>G	NP_003241.2:n.1110+56A>G
NM_199334.3:c.1166A>G	NP_955366.1:p.Lys389Arg
NM_001190918.2:c.1110+56A>G	NP_001177847.1:n.1110+56A>G
NM_003250.6:c.1110+56A>G	NP_003241.2:n.1110+56A>G
NM_199334.5:c.1166A>G MANE Select	NP_955366.1:p.Lys389Arg
NM_001190919.2:c.1110+56A>G	NP_001177848.1:n.1110+56A>G