Canonical Allele Identifier: CA2842489622

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50528584del , CM000684.2:g.50528584del	GRCh38
NC_000022.10:g.50967013del , CM000684.1:g.50967013del	GRCh37
NC_000022.9:g.49313879del	NCBI36
NG_011860.1:g.6505del , LRG_727:g.6505del
NG_016235.1:g.2859del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.447del MANE Select	ENSP00000252029.3:p.His150ThrfsTer?
ENST00000395680.6:c.447del	ENSP00000379037.1:p.His150ThrfsTer?
ENST00000395681.6:c.447del	ENSP00000379038.1:p.His150ThrfsTer?
ENST00000650719.1:c.447del	ENSP00000498276.1:p.His150ThrfsTer?
ENST00000651401.1:c.1-864del	ENSP00000499115.1:n.1-864del
ENST00000651906.1:n.566del
ENST00000652352.1:c.166-8del	ENSP00000498579.1:n.166-8del
ENST00000252029.7:c.447del	ENSP00000252029.3:p.His150ThrfsTer?
ENST00000395678.7:c.447del	ENSP00000379036.3:p.His150ThrfsTer?
ENST00000395680.5:c.447del	ENSP00000379037.1:p.His150ThrfsTer?
ENST00000395681.5:c.447del	ENSP00000379038.1:p.His150ThrfsTer?
ENST00000425169.1:c.417+555del	ENSP00000395875.1:n.417+555del
ENST00000476284.1:n.572del
ENST00000487162.1:n.1260del
ENST00000487577.5:n.734del
NM_001113755.2:c.447del	NP_001107227.1:p.His150ThrfsTer?
NM_001113756.2:c.447del	NP_001107228.1:p.His150ThrfsTer?
NM_001257988.1:c.447del , LRG_727t1:c.447del	NP_001244917.1:p.His150ThrfsTer?
NM_001257989.1:c.447del , LRG_727t2:c.447del	NP_001244918.1:p.His150ThrfsTer?
NM_001953.4:c.447del	NP_001944.1:p.His150ThrfsTer?
NM_001113755.3:c.447del	NP_001107227.1:p.His150ThrfsTer?
NM_001113756.3:c.447del	NP_001107228.1:p.His150ThrfsTer?
NM_001953.5:c.447del MANE Select	NP_001944.1:p.His150ThrfsTer?