Canonical Allele Identifier: CA2410908400
Gene: TYMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50527177C= , CM000684.2:g.50527177C= GRCh38
NC_000022.10:g.50965606C= , CM000684.1:g.50965606C= GRCh37
NC_000022.9:g.49312472C= NCBI36
NG_011860.1:g.7909G= , LRG_727:g.7909G=
NG_016235.1:g.4263G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.753G= MANE Select ENSP00000252029.3:p.Leu251=
ENST00000395680.6:c.753G= ENSP00000379037.1:p.Leu251=
ENST00000395681.6:c.753G= ENSP00000379038.1:p.Leu251=
ENST00000650719.1:c.646+411G= ENSP00000498276.1:n.646+411G=
ENST00000651401.1:c.237G= ENSP00000499115.1:p.Leu79=
ENST00000652352.1:c.464G= ENSP00000498579.1:n.464G=
ENST00000652401.1:c.254G=
ENST00000252029.7:c.753G= ENSP00000252029.3:p.Leu251=
ENST00000395678.7:c.753G= ENSP00000379036.3:p.Leu251=
ENST00000395680.5:c.753G= ENSP00000379037.1:p.Leu251=
ENST00000395681.5:c.753G= ENSP00000379038.1:p.Leu251=
ENST00000425169.1:c.654G= ENSP00000395875.1:p.Leu218=
ENST00000476284.1:n.771+411G=
ENST00000487577.5:n.1040G=
NM_001113755.2:c.753G= NP_001107227.1:p.Leu251=
NM_001113756.2:c.753G= NP_001107228.1:p.Leu251=
NM_001257988.1:c.753G= , LRG_727t1:c.753G= NP_001244917.1:p.Leu251=
NM_001257989.1:c.753G= , LRG_727t2:c.753G= NP_001244918.1:p.Leu251=
NM_001953.4:c.753G= NP_001944.1:p.Leu251=
NM_001113755.3:c.753G= NP_001107227.1:p.Leu251=
NM_001113756.3:c.753G= NP_001107228.1:p.Leu251=
NM_001953.5:c.753G= MANE Select NP_001944.1:p.Leu251=