Canonical Allele Identifier: CA2410908007
Gene: TYMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526577G= , CM000684.2:g.50526577G= GRCh38
NC_000022.10:g.50965006G= , CM000684.1:g.50965006G= GRCh37
NC_000022.9:g.49311872G= NCBI36
NG_011860.1:g.8509C= , LRG_727:g.8509C=
NG_016235.1:g.4863C=
NG_021419.1:g.23362G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.927C= MANE Select ENSP00000252029.3:p.Leu309=
ENST00000395680.6:c.927C= ENSP00000379037.1:p.Leu309=
ENST00000395681.6:c.927C= ENSP00000379038.1:p.Leu309=
ENST00000650719.1:c.808C= ENSP00000498276.1:p.Arg270=
ENST00000651401.1:c.411C= ENSP00000499115.1:p.Leu137=
ENST00000652401.1:c.428C=
ENST00000252029.7:c.927C= ENSP00000252029.3:p.Leu309=
ENST00000395678.7:c.927C= ENSP00000379036.3:p.Leu309=
ENST00000395680.5:c.927C= ENSP00000379037.1:p.Leu309=
ENST00000395681.5:c.927C= ENSP00000379038.1:p.Leu309=
ENST00000425169.1:c.828C= ENSP00000395875.1:p.Leu276=
ENST00000476284.1:n.933C=
ENST00000487577.5:n.1214C=
NM_001113755.2:c.927C= NP_001107227.1:p.Leu309=
NM_001113756.2:c.927C= NP_001107228.1:p.Leu309=
NM_001257988.1:c.927C= , LRG_727t1:c.927C= NP_001244917.1:p.Leu309=
NM_001257989.1:c.927C= , LRG_727t2:c.927C= NP_001244918.1:p.Leu309=
NM_001953.4:c.927C= NP_001944.1:p.Leu309=
NM_001113755.3:c.927C= NP_001107227.1:p.Leu309=
NM_001113756.3:c.927C= NP_001107228.1:p.Leu309=
NM_001953.5:c.927C= MANE Select NP_001944.1:p.Leu309=