Canonical Allele Identifier: CA2150060147

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81068085_81068086delinsGA , CM000676.2:g.81068085_81068086delinsGA	GRCh38
NC_000014.8:g.81534429_81534430delinsGA , CM000676.1:g.81534429_81534430delinsGA	GRCh37
NC_000014.7:g.80604182_80604183delinsGA	NCBI36
NG_009206.1:g.117561_117562delinsGA , LRG_523:g.117561_117562delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.243-169_243-168delinsGA MANE Select	ENSP00000298171.2:n.243-169_243-168delinsGA
ENST00000298171.6:c.243-169_243-168delinsGA	ENSP00000298171.2:n.243-169_243-168delinsGA
ENST00000342443.10:c.243-169_243-168delinsGA	ENSP00000340113.6:n.243-169_243-168delinsGA
ENST00000541158.6:c.243-169_243-168delinsGA	ENSP00000441235.2:n.243-169_243-168delinsGA
ENST00000553763.1:n.343-169_343-168delinsGA
ENST00000554263.5:c.243-169_243-168delinsGA	ENSP00000451202.1:n.243-169_243-168delinsGA
ENST00000554435.1:c.243-169_243-168delinsGA	ENSP00000450549.1:n.243-169_243-168delinsGA
ENST00000555326.5:c.243-169_243-168delinsGA	ENSP00000451092.1:n.243-169_243-168delinsGA
NM_000369.2:c.243-169_243-168delinsGA , LRG_523t1:c.243-169_243-168delinsGA	NP_000360.2:n.243-169_243-168delinsGA
NM_001018036.2:c.243-169_243-168delinsGA	NP_001018046.1:n.243-169_243-168delinsGA
NM_001142626.2:c.243-169_243-168delinsGA	NP_001136098.1:n.243-169_243-168delinsGA
XM_005268037.3:c.243-169_243-168delinsGA	XP_005268094.1:n.243-169_243-168delinsGA
XM_005268039.1:c.243-169_243-168delinsGA	XP_005268096.1:n.243-169_243-168delinsGA
XM_006720245.1:c.243-169_243-168delinsGA	XP_006720308.1:n.243-169_243-168delinsGA
XM_011537119.1:c.-86-169_-86-168delinsGA	XP_011535421.1:n.-86-169_-86-168delinsGA
XR_245790.3:n.3676-14270_3676-14269delinsTC
XR_944075.1:n.2549-14270_2549-14269delinsTC
XR_944076.1:n.1442-14270_1442-14269delinsTC
XR_944077.1:n.2455-14270_2455-14269delinsTC
XR_944078.1:n.2455-14270_2455-14269delinsTC
XM_005268037.4:c.243-169_243-168delinsGA	XP_005268094.1:n.243-169_243-168delinsGA
XM_011537119.2:c.-86-169_-86-168delinsGA	XP_011535421.1:n.-86-169_-86-168delinsGA
XR_001751018.2:n.1989-14270_1989-14269delinsTC
XR_001751019.2:n.1895-14270_1895-14269delinsTC
XR_001751020.2:n.886-14270_886-14269delinsTC
XR_001751021.1:n.4437-14270_4437-14269delinsTC
XR_001751022.1:n.3334-14270_3334-14269delinsTC
XR_001751023.1:n.4476-14270_4476-14269delinsTC
XR_001751024.2:n.1989-14270_1989-14269delinsTC
XR_944075.3:n.2613-14270_2613-14269delinsTC
NM_000369.4:c.243-169_243-168delinsGA	NP_000360.2:n.243-169_243-168delinsGA
NM_001018036.3:c.243-169_243-168delinsGA	NP_001018046.1:n.243-169_243-168delinsGA
NM_001142626.3:c.243-169_243-168delinsGA	NP_001136098.1:n.243-169_243-168delinsGA
NM_000369.5:c.243-169_243-168delinsGA MANE Select	NP_000360.2:n.243-169_243-168delinsGA