Canonical Allele Identifier: CA2410907998
Gene: TYMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526568C= , CM000684.2:g.50526568C= GRCh38
NC_000022.10:g.50964997C= , CM000684.1:g.50964997C= GRCh37
NC_000022.9:g.49311863C= NCBI36
NG_011860.1:g.8518G= , LRG_727:g.8518G=
NG_016235.1:g.4872G=
NG_021419.1:g.23353C=

Transcript Alleles

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