Canonical Allele Identifier: CA1190425387

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033902_115033904delinsTTA , CM000663.2:g.115033902_115033904delinsTTA	GRCh38
NC_000001.10:g.115576523_115576525delinsTTA , CM000663.1:g.115576523_115576525delinsTTA	GRCh37
NC_000001.9:g.115378046_115378048delinsTTA	NCBI36
NG_015891.1:g.9109_9111delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.163-71_163-69delinsTTA MANE Select	ENSP00000256592.1:n.163-71_163-69delinsTTA
ENST00000256592.2:c.163-71_163-69delinsTTA	ENSP00000256592.1:n.163-71_163-69delinsTTA
ENST00000369517.1:c.163-71_163-69delinsTTA	ENSP00000358530.1:n.163-71_163-69delinsTTA
NM_000549.4:c.163-71_163-69delinsTTA	NP_000540.2:n.163-71_163-69delinsTTA
XM_011542065.1:c.163-71_163-69delinsTTA	XP_011540367.1:n.163-71_163-69delinsTTA
XM_011542065.2:c.163-71_163-69delinsTTA	XP_011540367.1:n.163-71_163-69delinsTTA
NM_000549.5:c.163-71_163-69delinsTTA MANE Select	NP_000540.2:n.163-71_163-69delinsTTA