Canonical Allele Identifier: CA709005661

Gene: TSHR

Linked Data

• dbSNP Id: rs1397412613
• gnomAD v4: 14-81142902-GC-G
• MyVariant Identifiers: chr14:g.81609247del (hg19) ; chr14:g.81142903del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81142905del , CM000676.2:g.81142905del	GRCh38
NC_000014.8:g.81609249del , CM000676.1:g.81609249del	GRCh37
NC_000014.7:g.80679002del	NCBI36
NG_009206.1:g.192381del , LRG_523:g.192381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.882-35del MANE Select	ENSP00000298171.2:n.882-35del
ENST00000636454.1:n.800-35del
ENST00000298171.6:c.882-35del	ENSP00000298171.2:n.882-35del
ENST00000541158.6:c.882-35del	ENSP00000441235.2:n.882-35del
NM_000369.2:c.882-35del , LRG_523t1:c.882-35del	NP_000360.2:n.882-35del
XM_005268037.3:c.882-35del	XP_005268094.1:n.882-35del
XM_011537119.1:c.603-35del	XP_011535421.1:n.603-35del
XR_245790.3:n.2086+22290del
XR_429385.2:n.853+22290del
XR_429386.2:n.854+22290del
XR_944075.1:n.865+22290del
XR_944076.1:n.861+22290del
XR_944077.1:n.865+22290del
XR_944078.1:n.865+22290del
XR_944079.1:n.855+22290del
XM_005268037.4:c.882-35del	XP_005268094.1:n.882-35del
XM_011537119.2:c.603-35del	XP_011535421.1:n.603-35del
XR_001751021.1:n.2753+22290del
XR_001751022.1:n.2753+22290del
XR_001751023.1:n.2753+22290del
XR_944075.3:n.929+22290del
NM_000369.4:c.882-35del	NP_000360.2:n.882-35del
NM_000369.5:c.882-35del MANE Select	NP_000360.2:n.882-35del