Canonical Allele Identifier: CA2657565316
Gene: TYMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526558_50526572del , CM000684.2:g.50526558_50526572del GRCh38
NC_000022.10:g.50964987_50965001del , CM000684.1:g.50964987_50965001del GRCh37
NC_000022.9:g.49311853_49311867del NCBI36
NG_011860.1:g.8519_8533del , LRG_727:g.8519_8533del
NG_016235.1:g.4873_4887del
NG_021419.1:g.23343_23357del

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.928+9_928+23del MANE Select ENSP00000252029.3:n.928+9_928+23del
ENST00000395680.6:c.928+9_928+23del ENSP00000379037.1:n.928+9_928+23del
ENST00000395681.6:c.928+9_928+23del ENSP00000379038.1:n.928+9_928+23del
ENST00000650719.1:c.809+9_809+23del ENSP00000498276.1:n.809+9_809+23del
ENST00000651401.1:c.412+9_412+23del ENSP00000499115.1:n.412+9_412+23del
ENST00000652401.1:c.429+9_429+23del
ENST00000252029.7:c.928+9_928+23del ENSP00000252029.3:n.928+9_928+23del
ENST00000395678.7:c.928+9_928+23del ENSP00000379036.3:n.928+9_928+23del
ENST00000395680.5:c.928+9_928+23del ENSP00000379037.1:n.928+9_928+23del
ENST00000395681.5:c.928+9_928+23del ENSP00000379038.1:n.928+9_928+23del
ENST00000425169.1:c.829+9_829+23del ENSP00000395875.1:n.829+9_829+23del
ENST00000476284.1:n.934+9_934+23del
ENST00000487577.5:n.1215+9_1215+23del
NM_001113755.2:c.928+9_928+23del NP_001107227.1:n.928+9_928+23del
NM_001113756.2:c.928+9_928+23del NP_001107228.1:n.928+9_928+23del
NM_001257988.1:c.928+9_928+23del , LRG_727t1:c.928+9_928+23del NP_001244917.1:n.928+9_928+23del
NM_001257989.1:c.928+9_928+23del , LRG_727t2:c.928+9_928+23del NP_001244918.1:n.928+9_928+23del
NM_001953.4:c.928+9_928+23del NP_001944.1:n.928+9_928+23del
NM_001113755.3:c.928+9_928+23del NP_001107227.1:n.928+9_928+23del
NM_001113756.3:c.928+9_928+23del NP_001107228.1:n.928+9_928+23del
NM_001953.5:c.928+9_928+23del MANE Select NP_001944.1:n.928+9_928+23del