Canonical Allele Identifier: CA325561956

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50527191G>A , CM000684.2:g.50527191G>A	GRCh38
NC_000022.10:g.50965620G>A , CM000684.1:g.50965620G>A	GRCh37
NC_000022.9:g.49312486G>A	NCBI36
NG_011860.1:g.7895C>T , LRG_727:g.7895C>T
NG_016235.1:g.4249C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001953.5:c.739C>T MANE Select	NP_001944.1:p.Gln247Ter
ENST00000252029.8:c.739C>T MANE Select	ENSP00000252029.3:p.Gln247Ter
NM_001113755.2:c.739C>T	NP_001107227.1:p.Gln247Ter
NM_001113755.3:c.739C>T	NP_001107227.1:p.Gln247Ter
NM_001113756.2:c.739C>T	NP_001107228.1:p.Gln247Ter
NM_001113756.3:c.739C>T	NP_001107228.1:p.Gln247Ter
NM_001257988.1:c.739C>T , LRG_727t1:c.739C>T	NP_001244917.1:p.Gln247Ter
NM_001257989.1:c.739C>T , LRG_727t2:c.739C>T	NP_001244918.1:p.Gln247Ter
NM_001953.4:c.739C>T	NP_001944.1:p.Gln247Ter
ENST00000252029.7:c.739C>T	ENSP00000252029.3:p.Gln247Ter
ENST00000395678.7:c.739C>T	ENSP00000379036.3:p.Gln247Ter
ENST00000395680.5:c.739C>T	ENSP00000379037.1:p.Gln247Ter
ENST00000395680.6:c.739C>T	ENSP00000379037.1:p.Gln247Ter
ENST00000395681.5:c.739C>T	ENSP00000379038.1:p.Gln247Ter
ENST00000395681.6:c.739C>T	ENSP00000379038.1:p.Gln247Ter
ENST00000425169.1:c.640C>T	ENSP00000395875.1:p.Gln214Ter
ENST00000476284.1:n.771+397C>T
ENST00000487577.5:n.1026C>T
ENST00000650719.1:c.646+397C>T	ENSP00000498276.1:n.646+397C>T
ENST00000651401.1:c.223C>T	ENSP00000499115.1:p.Gln75Ter
ENST00000652352.1:c.450C>T	ENSP00000498579.1:n.450C>T
ENST00000652401.1:c.240C>T