Canonical Allele Identifier: CA2150074463

Gene: TSHR

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81142907_81142910delinsGCCT , CM000676.2:g.81142907_81142910delinsGCCT	GRCh38
NC_000014.8:g.81609251_81609254delinsGCCT , CM000676.1:g.81609251_81609254delinsGCCT	GRCh37
NC_000014.7:g.80679004_80679007delinsGCCT	NCBI36
NG_009206.1:g.192383_192386delinsGCCT , LRG_523:g.192383_192386delinsGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.882-33_882-30delinsGCCT MANE Select	ENSP00000298171.2:n.882-33_882-30delinsGCCT
ENST00000636454.1:n.800-33_800-30delinsGCCT
ENST00000298171.6:c.882-33_882-30delinsGCCT	ENSP00000298171.2:n.882-33_882-30delinsGCCT
ENST00000541158.6:c.882-33_882-30delinsGCCT	ENSP00000441235.2:n.882-33_882-30delinsGCCT
NM_000369.2:c.882-33_882-30delinsGCCT , LRG_523t1:c.882-33_882-30delinsGCCT	NP_000360.2:n.882-33_882-30delinsGCCT
XM_005268037.3:c.882-33_882-30delinsGCCT	XP_005268094.1:n.882-33_882-30delinsGCCT
XM_011537119.1:c.603-33_603-30delinsGCCT	XP_011535421.1:n.603-33_603-30delinsGCCT
XR_245790.3:n.2086+22283_2086+22286delinsAGGC
XR_429385.2:n.853+22283_853+22286delinsAGGC
XR_429386.2:n.854+22283_854+22286delinsAGGC
XR_944075.1:n.865+22283_865+22286delinsAGGC
XR_944076.1:n.861+22283_861+22286delinsAGGC
XR_944077.1:n.865+22283_865+22286delinsAGGC
XR_944078.1:n.865+22283_865+22286delinsAGGC
XR_944079.1:n.855+22283_855+22286delinsAGGC
XM_005268037.4:c.882-33_882-30delinsGCCT	XP_005268094.1:n.882-33_882-30delinsGCCT
XM_011537119.2:c.603-33_603-30delinsGCCT	XP_011535421.1:n.603-33_603-30delinsGCCT
XR_001751021.1:n.2753+22283_2753+22286delinsAGGC
XR_001751022.1:n.2753+22283_2753+22286delinsAGGC
XR_001751023.1:n.2753+22283_2753+22286delinsAGGC
XR_944075.3:n.929+22283_929+22286delinsAGGC
NM_000369.4:c.882-33_882-30delinsGCCT	NP_000360.2:n.882-33_882-30delinsGCCT
NM_000369.5:c.882-33_882-30delinsGCCT MANE Select	NP_000360.2:n.882-33_882-30delinsGCCT