Canonical Allele Identifier: CA1809864598

Gene: TRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087655T= , CM000670.2:g.109087655T=	GRCh38
NC_000008.10:g.110099884T= , CM000670.1:g.110099884T=	GRCh37
NC_000008.9:g.110169060T=	NCBI36
NG_017161.1:g.5209T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.143T= MANE Select	ENSP00000430711.2:p.Leu48=
ENST00000311762.2:c.143T=	ENSP00000309818.2:p.Leu48=
ENST00000518632.1:c.143T=	ENSP00000430711.1:p.Leu48=
NM_003301.5:c.143T=	NP_003292.1:p.Leu48=
XM_011517263.1:c.143T=	XP_011515565.1:p.Leu48=
XM_011517263.2:c.143T=	XP_011515565.1:p.Leu48=
NM_003301.7:c.143T= MANE Select	NP_003292.1:p.Leu48=