Canonical Allele Identifier: CA2579227956
Gene: TRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109087644_109087646del , CM000670.2:g.109087644_109087646del GRCh38
NC_000008.10:g.110099873_110099875del , CM000670.1:g.110099873_110099875del GRCh37
NC_000008.9:g.110169049_110169051del NCBI36
NG_017161.1:g.5198_5200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.132_134del MANE Select ENSP00000430711.2:p.Ile44del
ENST00000311762.2:c.132_134del ENSP00000309818.2:p.Ile44del
ENST00000518632.1:c.132_134del ENSP00000430711.1:p.Ile44del
NM_003301.5:c.132_134del NP_003292.1:p.Ile44del
XM_011517263.1:c.132_134del XP_011515565.1:p.Ile44del
XM_011517263.2:c.132_134del XP_011515565.1:p.Ile44del
NM_003301.7:c.132_134del MANE Select NP_003292.1:p.Ile44del