Canonical Allele Identifier: CA412201913

Gene: TYMP

Linked Data

• MyVariant Identifiers: chr22:g.50967570A>C (hg19) ; chr22:g.50529141A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529141A>C , CM000684.2:g.50529141A>C	GRCh38
NC_000022.10:g.50967570A>C , CM000684.1:g.50967570A>C	GRCh37
NC_000022.9:g.49314436A>C	NCBI36
NG_011860.1:g.5945T>G , LRG_727:g.5945T>G
NG_016235.1:g.2299T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.412T>G MANE Select	ENSP00000252029.3:p.Cys138Gly
ENST00000395680.6:c.412T>G	ENSP00000379037.1:p.Cys138Gly
ENST00000395681.6:c.412T>G	ENSP00000379038.1:p.Cys138Gly
ENST00000650719.1:c.412T>G	ENSP00000498276.1:p.Cys138Gly
ENST00000651095.1:n.551T>G
ENST00000651196.1:c.412T>G
ENST00000651401.1:c.-1+763T>G	ENSP00000499115.1:n.-1+763T>G
ENST00000651906.1:n.531T>G
ENST00000652237.1:n.688T>G
ENST00000652352.1:c.160T>G	ENSP00000498579.1:p.Cys54Gly
ENST00000252029.7:c.412T>G	ENSP00000252029.3:p.Cys138Gly
ENST00000395678.7:c.412T>G	ENSP00000379036.3:p.Cys138Gly
ENST00000395680.5:c.412T>G	ENSP00000379037.1:p.Cys138Gly
ENST00000395681.5:c.412T>G	ENSP00000379038.1:p.Cys138Gly
ENST00000425169.1:c.412T>G	ENSP00000395875.1:p.Cys138Gly
ENST00000476284.1:n.537T>G
ENST00000487162.1:n.700T>G
ENST00000487577.5:n.699T>G
NM_001113755.2:c.412T>G	NP_001107227.1:p.Cys138Gly
NM_001113756.2:c.412T>G	NP_001107228.1:p.Cys138Gly
NM_001257988.1:c.412T>G , LRG_727t1:c.412T>G	NP_001244917.1:p.Cys138Gly
NM_001257989.1:c.412T>G , LRG_727t2:c.412T>G	NP_001244918.1:p.Cys138Gly
NM_001953.4:c.412T>G	NP_001944.1:p.Cys138Gly
NM_001113755.3:c.412T>G	NP_001107227.1:p.Cys138Gly
NM_001113756.3:c.412T>G	NP_001107228.1:p.Cys138Gly
NM_001953.5:c.412T>G MANE Select	NP_001944.1:p.Cys138Gly