Canonical Allele Identifier: CA412201519

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50527714G>A , CM000684.2:g.50527714G>A	GRCh38
NC_000022.10:g.50966143G>A , CM000684.1:g.50966143G>A	GRCh37
NC_000022.9:g.49313009G>A	NCBI36
NG_011860.1:g.7372C>T , LRG_727:g.7372C>T
NG_016235.1:g.3726C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001953.5:c.520C>T MANE Select	NP_001944.1:p.Gln174Ter
ENST00000252029.8:c.520C>T MANE Select	ENSP00000252029.3:p.Gln174Ter
NM_001113755.2:c.520C>T	NP_001107227.1:p.Gln174Ter
NM_001113755.3:c.520C>T	NP_001107227.1:p.Gln174Ter
NM_001113756.2:c.520C>T	NP_001107228.1:p.Gln174Ter
NM_001113756.3:c.520C>T	NP_001107228.1:p.Gln174Ter
NM_001257988.1:c.520C>T , LRG_727t1:c.520C>T	NP_001244917.1:p.Gln174Ter
NM_001257989.1:c.520C>T , LRG_727t2:c.520C>T	NP_001244918.1:p.Gln174Ter
NM_001953.4:c.520C>T	NP_001944.1:p.Gln174Ter
ENST00000252029.7:c.520C>T	ENSP00000252029.3:p.Gln174Ter
ENST00000395678.7:c.520C>T	ENSP00000379036.3:p.Gln174Ter
ENST00000395680.5:c.520C>T	ENSP00000379037.1:p.Gln174Ter
ENST00000395680.6:c.520C>T	ENSP00000379037.1:p.Gln174Ter
ENST00000395681.5:c.520C>T	ENSP00000379038.1:p.Gln174Ter
ENST00000395681.6:c.520C>T	ENSP00000379038.1:p.Gln174Ter
ENST00000425169.1:c.421C>T	ENSP00000395875.1:p.Gln141Ter
ENST00000476284.1:n.645C>T
ENST00000487577.5:n.807C>T
ENST00000650719.1:c.520C>T	ENSP00000498276.1:p.Gln174Ter
ENST00000651401.1:c.4C>T	ENSP00000499115.1:p.Gln2Ter
ENST00000651906.1:n.639C>T
ENST00000652352.1:c.231C>T	ENSP00000498579.1:p.Cys77=