Canonical Allele Identifier: CA399277652

Gene: THRA

Linked Data

• MyVariant Identifiers: chr17:g.38245569C>T (hg19) ; chr17:g.40089316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40089316C>T , CM000679.2:g.40089316C>T	GRCh38
NC_000017.10:g.38245569C>T , CM000679.1:g.38245569C>T	GRCh37
NC_000017.9:g.35499095C>T	NCBI36
NG_023345.1:g.32124C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450525.7:c.1093C>T MANE Select	ENSP00000395641.3:p.Pro365Ser
ENST00000264637.8:c.1093C>T	ENSP00000264637.4:p.Pro365Ser
ENST00000394121.8:c.1093C>T	ENSP00000377679.4:p.Pro365Ser
ENST00000450525.6:c.1093C>T	ENSP00000395641.2:p.Pro365Ser
ENST00000546243.5:c.1093C>T	ENSP00000443972.1:p.Pro365Ser
ENST00000584985.5:c.1093C>T	ENSP00000463466.1:p.Pro365Ser
NM_001190918.1:c.1093C>T	NP_001177847.1:p.Pro365Ser
NM_001190919.1:c.1093C>T	NP_001177848.1:p.Pro365Ser
NM_003250.5:c.1093C>T	NP_003241.2:p.Pro365Ser
NM_199334.3:c.1093C>T	NP_955366.1:p.Pro365Ser
NM_001190918.2:c.1093C>T	NP_001177847.1:p.Pro365Ser
NM_003250.6:c.1093C>T	NP_003241.2:p.Pro365Ser
NM_199334.5:c.1093C>T MANE Select	NP_955366.1:p.Pro365Ser
NM_001190919.2:c.1093C>T	NP_001177848.1:p.Pro365Ser