Canonical Allele Identifier: CA2657566274
Gene: TYMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50528637_50528648del , CM000684.2:g.50528637_50528648del GRCh38
NC_000022.10:g.50967066_50967077del , CM000684.1:g.50967066_50967077del GRCh37
NC_000022.9:g.49313932_49313943del NCBI36
NG_011860.1:g.6445_6456del , LRG_727:g.6445_6456del
NG_016235.1:g.2799_2810del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252029.8:c.418-31_418-20del MANE Select ENSP00000252029.3:n.418-31_418-20del
ENST00000395680.6:c.418-31_418-20del ENSP00000379037.1:n.418-31_418-20del
ENST00000395681.6:c.418-31_418-20del ENSP00000379038.1:n.418-31_418-20del
ENST00000650719.1:c.418-31_418-20del ENSP00000498276.1:n.418-31_418-20del
ENST00000651401.1:c.1-924_1-913del ENSP00000499115.1:n.1-924_1-913del
ENST00000651906.1:n.537-31_537-20del
ENST00000652352.1:c.166-68_166-57del ENSP00000498579.1:n.166-68_166-57del
ENST00000252029.7:c.418-31_418-20del ENSP00000252029.3:n.418-31_418-20del
ENST00000395678.7:c.418-31_418-20del ENSP00000379036.3:n.418-31_418-20del
ENST00000395680.5:c.418-31_418-20del ENSP00000379037.1:n.418-31_418-20del
ENST00000395681.5:c.418-31_418-20del ENSP00000379038.1:n.418-31_418-20del
ENST00000425169.1:c.417+495_417+506del ENSP00000395875.1:n.417+495_417+506del
ENST00000476284.1:n.543-31_543-20del
ENST00000487162.1:n.1200_1211del
ENST00000487577.5:n.705-31_705-20del
NM_001113755.2:c.418-31_418-20del NP_001107227.1:n.418-31_418-20del
NM_001113756.2:c.418-31_418-20del NP_001107228.1:n.418-31_418-20del
NM_001257988.1:c.418-31_418-20del , LRG_727t1:c.418-31_418-20del NP_001244917.1:n.418-31_418-20del
NM_001257989.1:c.418-31_418-20del , LRG_727t2:c.418-31_418-20del NP_001244918.1:n.418-31_418-20del
NM_001953.4:c.418-31_418-20del NP_001944.1:n.418-31_418-20del
NM_001113755.3:c.418-31_418-20del NP_001107227.1:n.418-31_418-20del
NM_001113756.3:c.418-31_418-20del NP_001107228.1:n.418-31_418-20del
NM_001953.5:c.418-31_418-20del MANE Select NP_001944.1:n.418-31_418-20del