Canonical Allele Identifier: CA412202804
Gene: TYMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50529601G>C , CM000684.2:g.50529601G>C GRCh38
NC_000022.10:g.50968030G>C , CM000684.1:g.50968030G>C GRCh37
NC_000022.9:g.49314896G>C NCBI36
NG_011860.1:g.5485C>G , LRG_727:g.5485C>G
NG_016235.1:g.1839C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.109C>G MANE Select ENSP00000252029.3:p.Pro37Ala
ENST00000395680.6:c.109C>G ENSP00000379037.1:p.Pro37Ala
ENST00000395681.6:c.109C>G ENSP00000379038.1:p.Pro37Ala
ENST00000650719.1:c.109C>G ENSP00000498276.1:p.Pro37Ala
ENST00000651095.1:n.248C>G
ENST00000651196.1:c.109C>G ENSP00000499096.1:p.Pro37Ala
ENST00000651401.1:c.-1+303C>G ENSP00000499115.1:n.-1+303C>G
ENST00000651906.1:n.228C>G
ENST00000652237.1:n.228C>G
ENST00000252029.7:c.109C>G ENSP00000252029.3:p.Pro37Ala
ENST00000395678.7:c.109C>G ENSP00000379036.3:p.Pro37Ala
ENST00000395680.5:c.109C>G ENSP00000379037.1:p.Pro37Ala
ENST00000395681.5:c.109C>G ENSP00000379038.1:p.Pro37Ala
ENST00000425169.1:c.109C>G ENSP00000395875.1:p.Pro37Ala
ENST00000476284.1:n.234C>G
ENST00000487162.1:n.240C>G
ENST00000487577.5:n.396C>G
NM_001113755.2:c.109C>G NP_001107227.1:p.Pro37Ala
NM_001113756.2:c.109C>G NP_001107228.1:p.Pro37Ala
NM_001257988.1:c.109C>G , LRG_727t1:c.109C>G NP_001244917.1:p.Pro37Ala
NM_001257989.1:c.109C>G , LRG_727t2:c.109C>G NP_001244918.1:p.Pro37Ala
NM_001953.4:c.109C>G NP_001944.1:p.Pro37Ala
NM_001113755.3:c.109C>G NP_001107227.1:p.Pro37Ala
NM_001113756.3:c.109C>G NP_001107228.1:p.Pro37Ala
NM_001953.5:c.109C>G MANE Select NP_001944.1:p.Pro37Ala