Canonical Allele Identifier: CA2410909211
Gene: TYMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50528489G= , CM000684.2:g.50528489G= GRCh38
NC_000022.10:g.50966918G= , CM000684.1:g.50966918G= GRCh37
NC_000022.9:g.49313784G= NCBI36
NG_011860.1:g.6597C= , LRG_727:g.6597C=
NG_016235.1:g.2951C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.516+23C= MANE Select ENSP00000252029.3:n.516+23C=
ENST00000395680.6:c.516+23C= ENSP00000379037.1:n.516+23C=
ENST00000395681.6:c.516+23C= ENSP00000379038.1:n.516+23C=
ENST00000650719.1:c.516+23C= ENSP00000498276.1:n.516+23C=
ENST00000651401.1:c.1-772C= ENSP00000499115.1:n.1-772C=
ENST00000651906.1:n.635+23C=
ENST00000652352.1:c.227+23C= ENSP00000498579.1:n.227+23C=
ENST00000252029.7:c.516+23C= ENSP00000252029.3:n.516+23C=
ENST00000395678.7:c.516+23C= ENSP00000379036.3:n.516+23C=
ENST00000395680.5:c.516+23C= ENSP00000379037.1:n.516+23C=
ENST00000395681.5:c.516+23C= ENSP00000379038.1:n.516+23C=
ENST00000425169.1:c.417+647C= ENSP00000395875.1:n.417+647C=
ENST00000476284.1:n.641+23C=
ENST00000487162.1:n.1352C=
ENST00000487577.5:n.803+23C=
NM_001113755.2:c.516+23C= NP_001107227.1:n.516+23C=
NM_001113756.2:c.516+23C= NP_001107228.1:n.516+23C=
NM_001257988.1:c.516+23C= , LRG_727t1:c.516+23C= NP_001244917.1:n.516+23C=
NM_001257989.1:c.516+23C= , LRG_727t2:c.516+23C= NP_001244918.1:n.516+23C=
NM_001953.4:c.516+23C= NP_001944.1:n.516+23C=
NM_001113755.3:c.516+23C= NP_001107227.1:n.516+23C=
NM_001113756.3:c.516+23C= NP_001107228.1:n.516+23C=
NM_001953.5:c.516+23C= MANE Select NP_001944.1:n.516+23C=