Canonical Allele Identifier: CA412201872

Gene: TYMP

Linked Data

• MyVariant Identifiers: chr22:g.50967032A>C (hg19) ; chr22:g.50528603A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50528603A>C , CM000684.2:g.50528603A>C	GRCh38
NC_000022.10:g.50967032A>C , CM000684.1:g.50967032A>C	GRCh37
NC_000022.9:g.49313898A>C	NCBI36
NG_011860.1:g.6483T>G , LRG_727:g.6483T>G
NG_016235.1:g.2837T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.425T>G MANE Select	ENSP00000252029.3:p.Met142Arg
ENST00000395680.6:c.425T>G	ENSP00000379037.1:p.Met142Arg
ENST00000395681.6:c.425T>G	ENSP00000379038.1:p.Met142Arg
ENST00000650719.1:c.425T>G	ENSP00000498276.1:p.Met142Arg
ENST00000651401.1:c.1-886T>G	ENSP00000499115.1:n.1-886T>G
ENST00000651906.1:n.544T>G
ENST00000652352.1:c.166-30T>G	ENSP00000498579.1:n.166-30T>G
ENST00000252029.7:c.425T>G	ENSP00000252029.3:p.Met142Arg
ENST00000395678.7:c.425T>G	ENSP00000379036.3:p.Met142Arg
ENST00000395680.5:c.425T>G	ENSP00000379037.1:p.Met142Arg
ENST00000395681.5:c.425T>G	ENSP00000379038.1:p.Met142Arg
ENST00000425169.1:c.417+533T>G	ENSP00000395875.1:n.417+533T>G
ENST00000476284.1:n.550T>G
ENST00000487162.1:n.1238T>G
ENST00000487577.5:n.712T>G
NM_001113755.2:c.425T>G	NP_001107227.1:p.Met142Arg
NM_001113756.2:c.425T>G	NP_001107228.1:p.Met142Arg
NM_001257988.1:c.425T>G , LRG_727t1:c.425T>G	NP_001244917.1:p.Met142Arg
NM_001257989.1:c.425T>G , LRG_727t2:c.425T>G	NP_001244918.1:p.Met142Arg
NM_001953.4:c.425T>G	NP_001944.1:p.Met142Arg
NM_001113755.3:c.425T>G	NP_001107227.1:p.Met142Arg
NM_001113756.3:c.425T>G	NP_001107228.1:p.Met142Arg
NM_001953.5:c.425T>G MANE Select	NP_001944.1:p.Met142Arg