Canonical Allele Identifier: CA412199157
Gene: TYMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526665C>G , CM000684.2:g.50526665C>G GRCh38
NC_000022.10:g.50965094C>G , CM000684.1:g.50965094C>G GRCh37
NC_000022.9:g.49311960C>G NCBI36
NG_011860.1:g.8421G>C , LRG_727:g.8421G>C
NG_016235.1:g.4775G>C
NG_021419.1:g.23450C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.839G>C MANE Select ENSP00000252029.3:p.Cys280Ser
ENST00000395680.6:c.839G>C ENSP00000379037.1:p.Cys280Ser
ENST00000395681.6:c.839G>C ENSP00000379038.1:p.Cys280Ser
ENST00000650719.1:c.720G>C ENSP00000498276.1:p.Leu240=
ENST00000651401.1:c.323G>C ENSP00000499115.1:p.Cys108Ser
ENST00000652401.1:c.340G>C
ENST00000252029.7:c.839G>C ENSP00000252029.3:p.Cys280Ser
ENST00000395678.7:c.839G>C ENSP00000379036.3:p.Cys280Ser
ENST00000395680.5:c.839G>C ENSP00000379037.1:p.Cys280Ser
ENST00000395681.5:c.839G>C ENSP00000379038.1:p.Cys280Ser
ENST00000425169.1:c.740G>C ENSP00000395875.1:p.Cys247Ser
ENST00000476284.1:n.845G>C
ENST00000487577.5:n.1126G>C
NM_001113755.2:c.839G>C NP_001107227.1:p.Cys280Ser
NM_001113756.2:c.839G>C NP_001107228.1:p.Cys280Ser
NM_001257988.1:c.839G>C , LRG_727t1:c.839G>C NP_001244917.1:p.Cys280Ser
NM_001257989.1:c.839G>C , LRG_727t2:c.839G>C NP_001244918.1:p.Cys280Ser
NM_001953.4:c.839G>C NP_001944.1:p.Cys280Ser
NM_001113755.3:c.839G>C NP_001107227.1:p.Cys280Ser
NM_001113756.3:c.839G>C NP_001107228.1:p.Cys280Ser
NM_001953.5:c.839G>C MANE Select NP_001944.1:p.Cys280Ser