Canonical Allele Identifier: CA10575715

Gene: THRA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40089430G>A , CM000679.2:g.40089430G>A	GRCh38
NC_000017.10:g.38245683G>A , CM000679.1:g.38245683G>A	GRCh37
NC_000017.9:g.35499209G>A	NCBI36
NG_023345.1:g.32238G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450525.7:c.1207G>A MANE Select	ENSP00000395641.3:p.Glu403Lys
ENST00000264637.8:c.1110+97G>A	ENSP00000264637.4:n.1110+97G>A
ENST00000394121.8:c.1110+97G>A	ENSP00000377679.4:n.1110+97G>A
ENST00000450525.6:c.1207G>A	ENSP00000395641.2:p.Glu403Lys
ENST00000546243.5:c.1207G>A	ENSP00000443972.1:p.Glu403Lys
ENST00000584985.5:c.1110+97G>A	ENSP00000463466.1:n.1110+97G>A
NM_001190918.1:c.1110+97G>A	NP_001177847.1:n.1110+97G>A
NM_001190919.1:c.1110+97G>A	NP_001177848.1:n.1110+97G>A
NM_003250.5:c.1110+97G>A	NP_003241.2:n.1110+97G>A
NM_199334.3:c.1207G>A	NP_955366.1:p.Glu403Lys
NM_001190918.2:c.1110+97G>A	NP_001177847.1:n.1110+97G>A
NM_003250.6:c.1110+97G>A	NP_003241.2:n.1110+97G>A
NM_199334.5:c.1207G>A MANE Select	NP_955366.1:p.Glu403Lys
NM_001190919.2:c.1110+97G>A	NP_001177848.1:n.1110+97G>A