Canonical Allele Identifier: CA390730978

Gene: TSHR

Linked Data

• MyVariant Identifiers: chr14:g.81534627A>G (hg19) ; chr14:g.81068283A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81068283A>G , CM000676.2:g.81068283A>G	GRCh38
NC_000014.8:g.81534627A>G , CM000676.1:g.81534627A>G	GRCh37
NC_000014.7:g.80604380A>G	NCBI36
NG_009206.1:g.117759A>G , LRG_523:g.117759A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298171.7:c.272A>G MANE Select	ENSP00000298171.2:p.Gln91Arg
ENST00000298171.6:c.272A>G	ENSP00000298171.2:p.Gln91Arg
ENST00000342443.10:c.272A>G	ENSP00000340113.6:p.Gln91Arg
ENST00000541158.6:c.272A>G	ENSP00000441235.2:p.Gln91Arg
ENST00000553763.1:n.372A>G
ENST00000554263.5:c.272A>G	ENSP00000451202.1:p.Gln91Arg
ENST00000554435.1:c.272A>G	ENSP00000450549.1:p.Gln91Arg
ENST00000555326.5:c.272A>G	ENSP00000451092.1:p.Gln91Arg
NM_000369.2:c.272A>G , LRG_523t1:c.272A>G	NP_000360.2:p.Gln91Arg
NM_001018036.2:c.272A>G	NP_001018046.1:p.Gln91Arg
NM_001142626.2:c.272A>G	NP_001136098.1:p.Gln91Arg
XM_005268037.3:c.272A>G	XP_005268094.1:p.Gln91Arg
XM_005268039.1:c.272A>G	XP_005268096.1:p.Gln91Arg
XM_006720245.1:c.272A>G	XP_006720308.1:p.Gln91Arg
XM_011537119.1:c.-57A>G	XP_011535421.1:n.-57A>G
XR_245790.3:n.3676-14467T>C
XR_944075.1:n.2549-14467T>C
XR_944076.1:n.1442-14467T>C
XR_944077.1:n.2455-14467T>C
XR_944078.1:n.2455-14467T>C
XM_005268037.4:c.272A>G	XP_005268094.1:p.Gln91Arg
XM_011537119.2:c.-57A>G	XP_011535421.1:n.-57A>G
XR_001751018.2:n.1989-14467T>C
XR_001751019.2:n.1895-14467T>C
XR_001751020.2:n.886-14467T>C
XR_001751021.1:n.4437-14467T>C
XR_001751022.1:n.3334-14467T>C
XR_001751023.1:n.4476-14467T>C
XR_001751024.2:n.1989-14467T>C
XR_944075.3:n.2613-14467T>C
NM_000369.4:c.272A>G	NP_000360.2:p.Gln91Arg
NM_001018036.3:c.272A>G	NP_001018046.1:p.Gln91Arg
NM_001142626.3:c.272A>G	NP_001136098.1:p.Gln91Arg
NM_000369.5:c.272A>G MANE Select	NP_000360.2:p.Gln91Arg