Canonical Allele Identifier: CA2410908401
Gene: TYMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50527178A= , CM000684.2:g.50527178A= GRCh38
NC_000022.10:g.50965607A= , CM000684.1:g.50965607A= GRCh37
NC_000022.9:g.49312473A= NCBI36
NG_011860.1:g.7908T= , LRG_727:g.7908T=
NG_016235.1:g.4262T=

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.752T= MANE Select ENSP00000252029.3:p.Leu251=
ENST00000395680.6:c.752T= ENSP00000379037.1:p.Leu251=
ENST00000395681.6:c.752T= ENSP00000379038.1:p.Leu251=
ENST00000650719.1:c.646+410T= ENSP00000498276.1:n.646+410T=
ENST00000651401.1:c.236T= ENSP00000499115.1:p.Leu79=
ENST00000652352.1:c.463T= ENSP00000498579.1:n.463T=
ENST00000652401.1:c.253T=
ENST00000252029.7:c.752T= ENSP00000252029.3:p.Leu251=
ENST00000395678.7:c.752T= ENSP00000379036.3:p.Leu251=
ENST00000395680.5:c.752T= ENSP00000379037.1:p.Leu251=
ENST00000395681.5:c.752T= ENSP00000379038.1:p.Leu251=
ENST00000425169.1:c.653T= ENSP00000395875.1:p.Leu218=
ENST00000476284.1:n.771+410T=
ENST00000487577.5:n.1039T=
NM_001113755.2:c.752T= NP_001107227.1:p.Leu251=
NM_001113756.2:c.752T= NP_001107228.1:p.Leu251=
NM_001257988.1:c.752T= , LRG_727t1:c.752T= NP_001244917.1:p.Leu251=
NM_001257989.1:c.752T= , LRG_727t2:c.752T= NP_001244918.1:p.Leu251=
NM_001953.4:c.752T= NP_001944.1:p.Leu251=
NM_001113755.3:c.752T= NP_001107227.1:p.Leu251=
NM_001113756.3:c.752T= NP_001107228.1:p.Leu251=
NM_001953.5:c.752T= MANE Select NP_001944.1:p.Leu251=