Canonical Allele Identifier: CA2410909783

Gene: TYMP

Linked Data

• dbSNP Id: rs2069514717

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529527_50529529del , CM000684.2:g.50529527_50529529del	GRCh38
NC_000022.10:g.50967956_50967958del , CM000684.1:g.50967956_50967958del	GRCh37
NC_000022.9:g.49314822_49314824del	NCBI36
NG_011860.1:g.5560_5562del , LRG_727:g.5560_5562del
NG_016235.1:g.1914_1916del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.184_186del MANE Select	ENSP00000252029.3:p.Val62del
ENST00000395680.6:c.184_186del	ENSP00000379037.1:p.Val62del
ENST00000395681.6:c.184_186del	ENSP00000379038.1:p.Val62del
ENST00000650719.1:c.184_186del	ENSP00000498276.1:p.Val62del
ENST00000651095.1:n.323_325del
ENST00000651196.1:c.184_186del	ENSP00000499096.1:p.Val62del
ENST00000651401.1:c.-1+378_-1+380del	ENSP00000499115.1:n.-1+378_-1+380del
ENST00000651906.1:n.303_305del
ENST00000652237.1:n.303_305del
ENST00000252029.7:c.184_186del	ENSP00000252029.3:p.Val62del
ENST00000395678.7:c.184_186del	ENSP00000379036.3:p.Val62del
ENST00000395680.5:c.184_186del	ENSP00000379037.1:p.Val62del
ENST00000395681.5:c.184_186del	ENSP00000379038.1:p.Val62del
ENST00000425169.1:c.184_186del	ENSP00000395875.1:p.Val62del
ENST00000476284.1:n.309_311del
ENST00000487162.1:n.315_317del
ENST00000487577.5:n.471_473del
NM_001113755.2:c.184_186del	NP_001107227.1:p.Val62del
NM_001113756.2:c.184_186del	NP_001107228.1:p.Val62del
NM_001257988.1:c.184_186del , LRG_727t1:c.184_186del	NP_001244917.1:p.Val62del
NM_001257989.1:c.184_186del , LRG_727t2:c.184_186del	NP_001244918.1:p.Val62del
NM_001953.4:c.184_186del	NP_001944.1:p.Val62del
NM_001113755.3:c.184_186del	NP_001107227.1:p.Val62del
NM_001113756.3:c.184_186del	NP_001107228.1:p.Val62del
NM_001953.5:c.184_186del MANE Select	NP_001944.1:p.Val62del