Canonical Allele Identifier: CA412202838
Gene: TYMP HGNC NCBI

Linked Data

dbSNP Id: rs2069518794

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50529613G>A , CM000684.2:g.50529613G>A GRCh38
NC_000022.10:g.50968042G>A , CM000684.1:g.50968042G>A GRCh37
NC_000022.9:g.49314908G>A NCBI36
NG_011860.1:g.5473C>T , LRG_727:g.5473C>T
NG_016235.1:g.1827C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.97C>T MANE Select ENSP00000252029.3:p.Pro33Ser
ENST00000395680.6:c.97C>T ENSP00000379037.1:p.Pro33Ser
ENST00000395681.6:c.97C>T ENSP00000379038.1:p.Pro33Ser
ENST00000650719.1:c.97C>T ENSP00000498276.1:p.Pro33Ser
ENST00000651095.1:n.236C>T
ENST00000651196.1:c.97C>T ENSP00000499096.1:p.Pro33Ser
ENST00000651401.1:c.-1+291C>T ENSP00000499115.1:n.-1+291C>T
ENST00000651906.1:n.216C>T
ENST00000652237.1:n.216C>T
ENST00000252029.7:c.97C>T ENSP00000252029.3:p.Pro33Ser
ENST00000395678.7:c.97C>T ENSP00000379036.3:p.Pro33Ser
ENST00000395680.5:c.97C>T ENSP00000379037.1:p.Pro33Ser
ENST00000395681.5:c.97C>T ENSP00000379038.1:p.Pro33Ser
ENST00000425169.1:c.97C>T ENSP00000395875.1:p.Pro33Ser
ENST00000476284.1:n.222C>T
ENST00000487162.1:n.228C>T
ENST00000487577.5:n.384C>T
NM_001113755.2:c.97C>T NP_001107227.1:p.Pro33Ser
NM_001113756.2:c.97C>T NP_001107228.1:p.Pro33Ser
NM_001257988.1:c.97C>T , LRG_727t1:c.97C>T NP_001244917.1:p.Pro33Ser
NM_001257989.1:c.97C>T , LRG_727t2:c.97C>T NP_001244918.1:p.Pro33Ser
NM_001953.4:c.97C>T NP_001944.1:p.Pro33Ser
NM_001113755.3:c.97C>T NP_001107227.1:p.Pro33Ser
NM_001113756.3:c.97C>T NP_001107228.1:p.Pro33Ser
NM_001953.5:c.97C>T MANE Select NP_001944.1:p.Pro33Ser