Canonical Allele Identifier: CA2410909801

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529554C= , CM000684.2:g.50529554C=	GRCh38
NC_000022.10:g.50967983C= , CM000684.1:g.50967983C=	GRCh37
NC_000022.9:g.49314849C=	NCBI36
NG_011860.1:g.5532G= , LRG_727:g.5532G=
NG_016235.1:g.1886G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.156G= MANE Select	ENSP00000252029.3:p.Ala52=
ENST00000395680.6:c.156G=	ENSP00000379037.1:p.Ala52=
ENST00000395681.6:c.156G=	ENSP00000379038.1:p.Ala52=
ENST00000650719.1:c.156G=	ENSP00000498276.1:p.Ala52=
ENST00000651095.1:n.295G=
ENST00000651196.1:c.156G=	ENSP00000499096.1:p.Ala52=
ENST00000651401.1:c.-1+350G=	ENSP00000499115.1:n.-1+350G=
ENST00000651906.1:n.275G=
ENST00000652237.1:n.275G=
ENST00000252029.7:c.156G=	ENSP00000252029.3:p.Ala52=
ENST00000395678.7:c.156G=	ENSP00000379036.3:p.Ala52=
ENST00000395680.5:c.156G=	ENSP00000379037.1:p.Ala52=
ENST00000395681.5:c.156G=	ENSP00000379038.1:p.Ala52=
ENST00000425169.1:c.156G=	ENSP00000395875.1:p.Ala52=
ENST00000476284.1:n.281G=
ENST00000487162.1:n.287G=
ENST00000487577.5:n.443G=
NM_001113755.2:c.156G=	NP_001107227.1:p.Ala52=
NM_001113756.2:c.156G=	NP_001107228.1:p.Ala52=
NM_001257988.1:c.156G= , LRG_727t1:c.156G=	NP_001244917.1:p.Ala52=
NM_001257989.1:c.156G= , LRG_727t2:c.156G=	NP_001244918.1:p.Ala52=
NM_001953.4:c.156G=	NP_001944.1:p.Ala52=
NM_001113755.3:c.156G=	NP_001107227.1:p.Ala52=
NM_001113756.3:c.156G=	NP_001107228.1:p.Ala52=
NM_001953.5:c.156G= MANE Select	NP_001944.1:p.Ala52=