Canonical Allele Identifier: CA1190425374

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033859_115033860delinsTC , CM000663.2:g.115033859_115033860delinsTC	GRCh38
NC_000001.10:g.115576480_115576481delinsTC , CM000663.1:g.115576480_115576481delinsTC	GRCh37
NC_000001.9:g.115378003_115378004delinsTC	NCBI36
NG_015891.1:g.9066_9067delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.163-114_163-113delinsTC MANE Select	ENSP00000256592.1:n.163-114_163-113delinsTC
ENST00000256592.2:c.163-114_163-113delinsTC	ENSP00000256592.1:n.163-114_163-113delinsTC
ENST00000369517.1:c.163-114_163-113delinsTC	ENSP00000358530.1:n.163-114_163-113delinsTC
NM_000549.4:c.163-114_163-113delinsTC	NP_000540.2:n.163-114_163-113delinsTC
XM_011542065.1:c.163-114_163-113delinsTC	XP_011540367.1:n.163-114_163-113delinsTC
XM_011542065.2:c.163-114_163-113delinsTC	XP_011540367.1:n.163-114_163-113delinsTC
NM_000549.5:c.163-114_163-113delinsTC MANE Select	NP_000540.2:n.163-114_163-113delinsTC