Canonical Allele Identifier: CA16616779
Gene: TYMP HGNC NCBI

Linked Data

ClinVar Variation Id: 223029
ClinVar RCV Id: RCV000208704
dbSNP Id: rs1064792863

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50528561T>C , CM000684.2:g.50528561T>C GRCh38
NC_000022.10:g.50966990T>C , CM000684.1:g.50966990T>C GRCh37
NC_000022.9:g.49313856T>C NCBI36
NG_011860.1:g.6525A>G , LRG_727:g.6525A>G
NG_016235.1:g.2879A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252029.8:c.467A>G MANE Select ENSP00000252029.3:p.Asp156Gly
ENST00000395680.6:c.467A>G ENSP00000379037.1:p.Asp156Gly
ENST00000395681.6:c.467A>G ENSP00000379038.1:p.Asp156Gly
ENST00000650719.1:c.467A>G ENSP00000498276.1:p.Asp156Gly
ENST00000651401.1:c.1-844A>G ENSP00000499115.1:n.1-844A>G
ENST00000651906.1:n.586A>G
ENST00000652352.1:c.178A>G ENSP00000498579.1:p.Ile60Val
ENST00000252029.7:c.467A>G ENSP00000252029.3:p.Asp156Gly
ENST00000395678.7:c.467A>G ENSP00000379036.3:p.Asp156Gly
ENST00000395680.5:c.467A>G ENSP00000379037.1:p.Asp156Gly
ENST00000395681.5:c.467A>G ENSP00000379038.1:p.Asp156Gly
ENST00000425169.1:c.417+575A>G ENSP00000395875.1:n.417+575A>G
ENST00000476284.1:n.592A>G
ENST00000487162.1:n.1280A>G
ENST00000487577.5:n.754A>G
NM_001113755.2:c.467A>G NP_001107227.1:p.Asp156Gly
NM_001113756.2:c.467A>G NP_001107228.1:p.Asp156Gly
NM_001257988.1:c.467A>G , LRG_727t1:c.467A>G NP_001244917.1:p.Asp156Gly
NM_001257989.1:c.467A>G , LRG_727t2:c.467A>G NP_001244918.1:p.Asp156Gly
NM_001953.4:c.467A>G NP_001944.1:p.Asp156Gly
NM_001113755.3:c.467A>G NP_001107227.1:p.Asp156Gly
NM_001113756.3:c.467A>G NP_001107228.1:p.Asp156Gly
NM_001953.5:c.467A>G MANE Select NP_001944.1:p.Asp156Gly