Canonical Allele Identifier: CA2410909569

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529159C= , CM000684.2:g.50529159C=	GRCh38
NC_000022.10:g.50967588C= , CM000684.1:g.50967588C=	GRCh37
NC_000022.9:g.49314454C=	NCBI36
NG_011860.1:g.5927G= , LRG_727:g.5927G=
NG_016235.1:g.2281G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.394G= MANE Select	ENSP00000252029.3:p.Ala132=
ENST00000395680.6:c.394G=	ENSP00000379037.1:p.Ala132=
ENST00000395681.6:c.394G=	ENSP00000379038.1:p.Ala132=
ENST00000650719.1:c.394G=	ENSP00000498276.1:p.Ala132=
ENST00000651095.1:n.533G=
ENST00000651196.1:c.394G=	ENSP00000499096.1:p.Ala132=
ENST00000651401.1:c.-1+745G=	ENSP00000499115.1:n.-1+745G=
ENST00000651906.1:n.513G=
ENST00000652237.1:n.670G=
ENST00000652352.1:c.142G=	ENSP00000498579.1:p.Ala48=
ENST00000252029.7:c.394G=	ENSP00000252029.3:p.Ala132=
ENST00000395678.7:c.394G=	ENSP00000379036.3:p.Ala132=
ENST00000395680.5:c.394G=	ENSP00000379037.1:p.Ala132=
ENST00000395681.5:c.394G=	ENSP00000379038.1:p.Ala132=
ENST00000425169.1:c.394G=	ENSP00000395875.1:p.Ala132=
ENST00000476284.1:n.519G=
ENST00000487162.1:n.682G=
ENST00000487577.5:n.681G=
NM_001113755.2:c.394G=	NP_001107227.1:p.Ala132=
NM_001113756.2:c.394G=	NP_001107228.1:p.Ala132=
NM_001257988.1:c.394G= , LRG_727t1:c.394G=	NP_001244917.1:p.Ala132=
NM_001257989.1:c.394G= , LRG_727t2:c.394G=	NP_001244918.1:p.Ala132=
NM_001953.4:c.394G=	NP_001944.1:p.Ala132=
NM_001113755.3:c.394G=	NP_001107227.1:p.Ala132=
NM_001113756.3:c.394G=	NP_001107228.1:p.Ala132=
NM_001953.5:c.394G= MANE Select	NP_001944.1:p.Ala132=