Canonical Allele Identifier: CA1190425314

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033720_115033722delinsAAC , CM000663.2:g.115033720_115033722delinsAAC	GRCh38
NC_000001.10:g.115576341_115576343delinsAAC , CM000663.1:g.115576341_115576343delinsAAC	GRCh37
NC_000001.9:g.115377864_115377866delinsAAC	NCBI36
NG_015891.1:g.8927_8929delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+196_162+198delinsAAC MANE Select	ENSP00000256592.1:n.162+196_162+198delinsAAC
ENST00000256592.2:c.162+196_162+198delinsAAC	ENSP00000256592.1:n.162+196_162+198delinsAAC
ENST00000369517.1:c.162+196_162+198delinsAAC	ENSP00000358530.1:n.162+196_162+198delinsAAC
NM_000549.4:c.162+196_162+198delinsAAC	NP_000540.2:n.162+196_162+198delinsAAC
XM_011542065.1:c.162+196_162+198delinsAAC	XP_011540367.1:n.162+196_162+198delinsAAC
XM_011542065.2:c.162+196_162+198delinsAAC	XP_011540367.1:n.162+196_162+198delinsAAC
NM_000549.5:c.162+196_162+198delinsAAC MANE Select	NP_000540.2:n.162+196_162+198delinsAAC