Canonical Allele Identifier: CA412202648

Gene: TYMP

Linked Data

• MyVariant Identifiers: chr22:g.50967991T>C (hg19) ; chr22:g.50529562T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529562T>C , CM000684.2:g.50529562T>C	GRCh38
NC_000022.10:g.50967991T>C , CM000684.1:g.50967991T>C	GRCh37
NC_000022.9:g.49314857T>C	NCBI36
NG_011860.1:g.5524A>G , LRG_727:g.5524A>G
NG_016235.1:g.1878A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.148A>G MANE Select	ENSP00000252029.3:p.Ser50Gly
ENST00000395680.6:c.148A>G	ENSP00000379037.1:p.Ser50Gly
ENST00000395681.6:c.148A>G	ENSP00000379038.1:p.Ser50Gly
ENST00000650719.1:c.148A>G	ENSP00000498276.1:p.Ser50Gly
ENST00000651095.1:n.287A>G
ENST00000651196.1:c.148A>G	ENSP00000499096.1:p.Ser50Gly
ENST00000651401.1:c.-1+342A>G	ENSP00000499115.1:n.-1+342A>G
ENST00000651906.1:n.267A>G
ENST00000652237.1:n.267A>G
ENST00000252029.7:c.148A>G	ENSP00000252029.3:p.Ser50Gly
ENST00000395678.7:c.148A>G	ENSP00000379036.3:p.Ser50Gly
ENST00000395680.5:c.148A>G	ENSP00000379037.1:p.Ser50Gly
ENST00000395681.5:c.148A>G	ENSP00000379038.1:p.Ser50Gly
ENST00000425169.1:c.148A>G	ENSP00000395875.1:p.Ser50Gly
ENST00000476284.1:n.273A>G
ENST00000487162.1:n.279A>G
ENST00000487577.5:n.435A>G
NM_001113755.2:c.148A>G	NP_001107227.1:p.Ser50Gly
NM_001113756.2:c.148A>G	NP_001107228.1:p.Ser50Gly
NM_001257988.1:c.148A>G , LRG_727t1:c.148A>G	NP_001244917.1:p.Ser50Gly
NM_001257989.1:c.148A>G , LRG_727t2:c.148A>G	NP_001244918.1:p.Ser50Gly
NM_001953.4:c.148A>G	NP_001944.1:p.Ser50Gly
NM_001113755.3:c.148A>G	NP_001107227.1:p.Ser50Gly
NM_001113756.3:c.148A>G	NP_001107228.1:p.Ser50Gly
NM_001953.5:c.148A>G MANE Select	NP_001944.1:p.Ser50Gly