Canonical Allele Identifier: CA2563307904
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033867_115033868insATCATGGGAACAAGATAAGGT , CM000663.2:g.115033867_115033868insATCATGGGAACAAGATAAGGT GRCh38
NC_000001.10:g.115576488_115576489insATCATGGGAACAAGATAAGGT , CM000663.1:g.115576488_115576489insATCATGGGAACAAGATAAGGT GRCh37
NC_000001.9:g.115378011_115378012insATCATGGGAACAAGATAAGGT NCBI36
NG_015891.1:g.9074_9075insATCATGGGAACAAGATAAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-106_163-105insATCATGGGAACAAGATAAGGT MANE Select ENSP00000256592.1:n.163-106_163-105insATCATGGGAACAAGATAAGGT
ENST00000256592.2:c.163-106_163-105insATCATGGGAACAAGATAAGGT ENSP00000256592.1:n.163-106_163-105insATCATGGGAACAAGATAAGGT
ENST00000369517.1:c.163-106_163-105insATCATGGGAACAAGATAAGGT ENSP00000358530.1:n.163-106_163-105insATCATGGGAACAAGATAAGGT
NM_000549.4:c.163-106_163-105insATCATGGGAACAAGATAAGGT NP_000540.2:n.163-106_163-105insATCATGGGAACAAGATAAGGT
XM_011542065.1:c.163-106_163-105insATCATGGGAACAAGATAAGGT XP_011540367.1:n.163-106_163-105insATCATGGGAACAAGATAAGGT
XM_011542065.2:c.163-106_163-105insATCATGGGAACAAGATAAGGT XP_011540367.1:n.163-106_163-105insATCATGGGAACAAGATAAGGT
NM_000549.5:c.163-106_163-105insATCATGGGAACAAGATAAGGT MANE Select NP_000540.2:n.163-106_163-105insATCATGGGAACAAGATAAGGT