Canonical Allele Identifier: CA487339686

Gene: TSHR

Linked Data

• dbSNP Id: rs749182960
• MyVariant Identifiers: chr14:g.81534622G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81068278G>C , CM000676.2:g.81068278G>C	GRCh38
NC_000014.8:g.81534622G>C , CM000676.1:g.81534622G>C	GRCh37
NC_000014.7:g.80604375G>C	NCBI36
NG_009206.1:g.117754G>C , LRG_523:g.117754G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298171.7:c.267G>C MANE Select	ENSP00000298171.2:p.Leu89=
ENST00000298171.6:c.267G>C	ENSP00000298171.2:p.Leu89=
ENST00000342443.10:c.267G>C	ENSP00000340113.6:p.Leu89=
ENST00000541158.6:c.267G>C	ENSP00000441235.2:p.Leu89=
ENST00000553763.1:n.367G>C
ENST00000554263.5:c.267G>C	ENSP00000451202.1:p.Leu89=
ENST00000554435.1:c.267G>C	ENSP00000450549.1:p.Leu89=
ENST00000555326.5:c.267G>C	ENSP00000451092.1:p.Leu89=
NM_000369.2:c.267G>C , LRG_523t1:c.267G>C	NP_000360.2:p.Leu89=
NM_001018036.2:c.267G>C	NP_001018046.1:p.Leu89=
NM_001142626.2:c.267G>C	NP_001136098.1:p.Leu89=
XM_005268037.3:c.267G>C	XP_005268094.1:p.Leu89=
XM_005268039.1:c.267G>C	XP_005268096.1:p.Leu89=
XM_006720245.1:c.267G>C	XP_006720308.1:p.Leu89=
XM_011537119.1:c.-62G>C	XP_011535421.1:n.-62G>C
XR_245790.3:n.3676-14462C>G
XR_944075.1:n.2549-14462C>G
XR_944076.1:n.1442-14462C>G
XR_944077.1:n.2455-14462C>G
XR_944078.1:n.2455-14462C>G
XM_005268037.4:c.267G>C	XP_005268094.1:p.Leu89=
XM_011537119.2:c.-62G>C	XP_011535421.1:n.-62G>C
XR_001751018.2:n.1989-14462C>G
XR_001751019.2:n.1895-14462C>G
XR_001751020.2:n.886-14462C>G
XR_001751021.1:n.4437-14462C>G
XR_001751022.1:n.3334-14462C>G
XR_001751023.1:n.4476-14462C>G
XR_001751024.2:n.1989-14462C>G
XR_944075.3:n.2613-14462C>G
NM_000369.4:c.267G>C	NP_000360.2:p.Leu89=
NM_001018036.3:c.267G>C	NP_001018046.1:p.Leu89=
NM_001142626.3:c.267G>C	NP_001136098.1:p.Leu89=
NM_000369.5:c.267G>C MANE Select	NP_000360.2:p.Leu89=